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Biosense Webster® QWIKCABLE® Autoclavable extension cable
EUDAMEDFDA UDIClass I (EU MDR)
Ref C6MRMST4SA
Identity
- Trade Name
- Biosense Webster® QWIKCABLE® Autoclavable extension cable EUDAMEDBiosense Webster FDA UDI
- Generic Name
- Electrical-only medical device connection cable, reusable FDA UDI
- Device Name
- Reusable Diagnostic Extension Cables EUDAMEDBiosense Webster® QWIKCABLE® Autoclavable extension cable D-1221-22-S / 39F-55R FDA UDI
- Model / Reference
- C6MRMST4SA EUDAMEDFDA UDI
- Description
- Biosense Webster® QWIKCABLE® Autoclavable extension cable D-1221-22-S / 39F-55R FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08718375860175 EUDAMEDFDA UDI
- Basic UDI-DI
- B-08718375860175 EUDAMED
- FDA Product Code
- IKD FDA UDI
- EMDN Code
- C010380 ARTERIAL CANNULAS - ACCESSORIES EUDAMED
- GMDN Term
- Electrical-only medical device connection cable, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 890.1175 FDA UDI
- Market of Registration
- Netherlands EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Ethylene Oxide FDA UDI
MR Unsafe FDA UDI
Biosense Webster® QWIKCABLE® Autoclavable extension cable by Technomed Europe — Class I — MDD, FDA UDI — listed in EUDAMED, FDA GUDID
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-08718375860175 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Technomed Europe
- EUDAMED SRN
- NL-MF-000000064
Sources (2)
- EUDAMED 49594f98-0bf5-4f1b-ae6a-3836c5652a96 61 fields · synced Jun 18, 2026
- FDA UDI 16b4087b-8f68-4e00-87ea-3b67210d40da 34 fields · synced May 30, 2026