<?xml version="1.0" encoding="UTF-8"?>
<eudamedExport entity="devices">
  <row>
    <udiDi>20886333005783</udiDi>
    <basicUdiDi>0886333010006XP</basicUdiDi>
    <tradeName>Skater</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Argon Medical Devices, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000002324</manufacturerSrn>
    <authorisedRepresentativeName>Emergo Europe B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000116</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>A060204</emdnCode>
    <emdnDescription>THORACENTESIS AND PARACENTESIS DRAINAGES AND KITS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>700304015</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-20T22:14:41.445Z</lastUpdated>
  </row>
  <row>
    <udiDi>20886333005790</udiDi>
    <basicUdiDi>0886333010006XP</basicUdiDi>
    <tradeName>Skater</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Argon Medical Devices, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000002324</manufacturerSrn>
    <authorisedRepresentativeName>Emergo Europe B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000116</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>A060204</emdnCode>
    <emdnDescription>THORACENTESIS AND PARACENTESIS DRAINAGES AND KITS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>700305007</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-20T22:14:41.417Z</lastUpdated>
  </row>
  <row>
    <udiDi>20886333005806</udiDi>
    <basicUdiDi>0886333010006XP</basicUdiDi>
    <tradeName>Skater</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Argon Medical Devices, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000002324</manufacturerSrn>
    <authorisedRepresentativeName>Emergo Europe B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000116</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>A060204</emdnCode>
    <emdnDescription>THORACENTESIS AND PARACENTESIS DRAINAGES AND KITS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>700305010</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-20T22:14:41.395Z</lastUpdated>
  </row>
  <row>
    <udiDi>20886333005813</udiDi>
    <basicUdiDi>0886333010006XP</basicUdiDi>
    <tradeName>Skater</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Argon Medical Devices, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000002324</manufacturerSrn>
    <authorisedRepresentativeName>Emergo Europe B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000116</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>A060204</emdnCode>
    <emdnDescription>THORACENTESIS AND PARACENTESIS DRAINAGES AND KITS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>700305020</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-20T22:14:41.374Z</lastUpdated>
  </row>
  <row>
    <udiDi>20886333223330</udiDi>
    <basicUdiDi>0886333010014XN</basicUdiDi>
    <tradeName>Skater</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Argon Medical Devices, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000002324</manufacturerSrn>
    <authorisedRepresentativeName>Emergo Europe B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000116</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>A0680</emdnCode>
    <emdnDescription>DRAINAGE AND FLUID COLLECTION DEVICES - ACCESSORIES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>651006000</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-20T22:14:39.553Z</lastUpdated>
  </row>
  <row>
    <udiDi>20886333223354</udiDi>
    <basicUdiDi>0886333010014XN</basicUdiDi>
    <tradeName>Skater</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Argon Medical Devices, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000002324</manufacturerSrn>
    <authorisedRepresentativeName>Emergo Europe B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000116</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>A0680</emdnCode>
    <emdnDescription>DRAINAGE AND FLUID COLLECTION DEVICES - ACCESSORIES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>651006300</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-20T22:14:39.541Z</lastUpdated>
  </row>
  <row>
    <udiDi>10886333210999</udiDi>
    <basicUdiDi>08863332700022E</basicUdiDi>
    <tradeName>Guidewire</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Argon Medical Devices, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000002324</manufacturerSrn>
    <authorisedRepresentativeName>Emergo Europe B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000116</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C04020102</emdnCode>
    <emdnDescription>PERIPHERAL VASCULAR DIAGNOSTIC GUIDEWIRES, NON-HYDROPHILIC</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>395206</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-16T04:51:35.378Z</lastUpdated>
  </row>
  <row>
    <udiDi>10886333211507</udiDi>
    <basicUdiDi>08863332700022E</basicUdiDi>
    <tradeName>Guidewire</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Argon Medical Devices, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000002324</manufacturerSrn>
    <authorisedRepresentativeName>Emergo Europe B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000116</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C04020102</emdnCode>
    <emdnDescription>PERIPHERAL VASCULAR DIAGNOSTIC GUIDEWIRES, NON-HYDROPHILIC</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>395451</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-16T04:51:35.350Z</lastUpdated>
  </row>
  <row>
    <udiDi>10886333211613</udiDi>
    <basicUdiDi>08863332700022E</basicUdiDi>
    <tradeName>Guidewire</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Argon Medical Devices, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000002324</manufacturerSrn>
    <authorisedRepresentativeName>Emergo Europe B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000116</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C04020102</emdnCode>
    <emdnDescription>PERIPHERAL VASCULAR DIAGNOSTIC GUIDEWIRES, NON-HYDROPHILIC</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>395513</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-16T04:51:35.338Z</lastUpdated>
  </row>
  <row>
    <udiDi>10886333211651</udiDi>
    <basicUdiDi>08863332700022E</basicUdiDi>
    <tradeName>Guidewire</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Argon Medical Devices, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000002324</manufacturerSrn>
    <authorisedRepresentativeName>Emergo Europe B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000116</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C04020102</emdnCode>
    <emdnDescription>PERIPHERAL VASCULAR DIAGNOSTIC GUIDEWIRES, NON-HYDROPHILIC</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>395536</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-16T04:51:35.323Z</lastUpdated>
  </row>
  <row>
    <udiDi>10886333211705</udiDi>
    <basicUdiDi>08863332700062N</basicUdiDi>
    <tradeName>Guidewire</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Argon Medical Devices, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000002324</manufacturerSrn>
    <authorisedRepresentativeName>Emergo Europe B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000116</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>A060299</emdnCode>
    <emdnDescription>PERCUTANEOUS DRAINAGE SYSTEMS - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>395573</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-16T04:51:35.300Z</lastUpdated>
  </row>
  <row>
    <udiDi>10886333211743</udiDi>
    <basicUdiDi>08863332700062N</basicUdiDi>
    <tradeName>Guidewire</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Argon Medical Devices, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000002324</manufacturerSrn>
    <authorisedRepresentativeName>Emergo Europe B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000116</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>A060299</emdnCode>
    <emdnDescription>PERCUTANEOUS DRAINAGE SYSTEMS - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>395610</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-16T04:51:35.288Z</lastUpdated>
  </row>
  <row>
    <udiDi>10886333211774</udiDi>
    <basicUdiDi>08863332700062N</basicUdiDi>
    <tradeName>Guidewire</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Argon Medical Devices, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000002324</manufacturerSrn>
    <authorisedRepresentativeName>Emergo Europe B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000116</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>A060299</emdnCode>
    <emdnDescription>PERCUTANEOUS DRAINAGE SYSTEMS - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>395654</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-16T04:51:35.273Z</lastUpdated>
  </row>
  <row>
    <udiDi>10886333211798</udiDi>
    <basicUdiDi>08863332700102D</basicUdiDi>
    <tradeName>Guidewire</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Argon Medical Devices, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000002324</manufacturerSrn>
    <authorisedRepresentativeName>Emergo Europe B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000116</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C04020102</emdnCode>
    <emdnDescription>PERIPHERAL VASCULAR DIAGNOSTIC GUIDEWIRES, NON-HYDROPHILIC</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>395680</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-16T04:51:35.252Z</lastUpdated>
  </row>
  <row>
    <udiDi>10886333211903</udiDi>
    <basicUdiDi>08863332700062N</basicUdiDi>
    <tradeName>Guidewire</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Argon Medical Devices, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000002324</manufacturerSrn>
    <authorisedRepresentativeName>Emergo Europe B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000116</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>A060299</emdnCode>
    <emdnDescription>PERCUTANEOUS DRAINAGE SYSTEMS - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>395746</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-16T04:51:35.229Z</lastUpdated>
  </row>
  <row>
    <udiDi>10886333211910</udiDi>
    <basicUdiDi>08863332700062N</basicUdiDi>
    <tradeName>Guidewire</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Argon Medical Devices, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000002324</manufacturerSrn>
    <authorisedRepresentativeName>Emergo Europe B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000116</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>A060299</emdnCode>
    <emdnDescription>PERCUTANEOUS DRAINAGE SYSTEMS - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>395752</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-16T04:51:35.208Z</lastUpdated>
  </row>
  <row>
    <udiDi>10886333211934</udiDi>
    <basicUdiDi>08863332700022E</basicUdiDi>
    <tradeName>Guidewire</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Argon Medical Devices, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000002324</manufacturerSrn>
    <authorisedRepresentativeName>Emergo Europe B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000116</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C04020102</emdnCode>
    <emdnDescription>PERIPHERAL VASCULAR DIAGNOSTIC GUIDEWIRES, NON-HYDROPHILIC</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>395770</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-16T04:51:35.183Z</lastUpdated>
  </row>
  <row>
    <udiDi>00886333225729</udiDi>
    <basicUdiDi>088633335000225</basicUdiDi>
    <tradeName>Scorpion</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Argon Medical Devices, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000002324</manufacturerSrn>
    <authorisedRepresentativeName>Emergo Europe B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000116</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C0104020208</emdnCode>
    <emdnDescription>TRANSJUGULAR INTRAHEPATIC PORTOSYSTEMIC SHUNT (TIPS) PERCUTANEOUS SYSTEMS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference></reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-07T14:15:41.326Z</lastUpdated>
  </row>
  <row>
    <udiDi>00886333224647</udiDi>
    <basicUdiDi>088633335000123</basicUdiDi>
    <tradeName>Traveler</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Argon Medical Devices, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000002324</manufacturerSrn>
    <authorisedRepresentativeName>Emergo Europe B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000116</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C0104020208</emdnCode>
    <emdnDescription>TRANSJUGULAR INTRAHEPATIC PORTOSYSTEMIC SHUNT (TIPS) PERCUTANEOUS SYSTEMS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference></reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-07T14:15:39.102Z</lastUpdated>
  </row>
  <row>
    <udiDi>00886333224630</udiDi>
    <basicUdiDi>088633335000123</basicUdiDi>
    <tradeName>Traveler</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Argon Medical Devices, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000002324</manufacturerSrn>
    <authorisedRepresentativeName>Emergo Europe B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000116</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C0104020208</emdnCode>
    <emdnDescription>TRANSJUGULAR INTRAHEPATIC PORTOSYSTEMIC SHUNT (TIPS) PERCUTANEOUS SYSTEMS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference></reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-07T14:15:37.994Z</lastUpdated>
  </row>
</eudamedExport>