← Back to catalogue
DORO COBRA® Quick-Clamp for Radiolucent Quick-Rail®
EUDAMEDFDA UDIClass I (EU MDR)
Ref 1201.022
Identity
- Trade Name
- DORO COBRA® Quick-Clamp for Radiolucent Quick-Rail® EUDAMEDDORO COBRA® Quick-Clamp FDA UDI
- Generic Name
- Surgical retraction system, reusable FDA UDI
- Device Name
- Retractor System EUDAMEDDORO COBRA® Quick-Clamp for Radiolucent Quick-Rail® FDA UDI
- Model / Reference
- 1201.022 EUDAMEDFDA UDI
- Description
- DORO COBRA® Quick-Clamp for Radiolucent Quick-Rail® FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04250435526859 EUDAMEDFDA UDI
- Basic UDI-DI
- 42504355PA04EP EUDAMED
- Direct Marketing DI
- 04250435526859 EUDAMED
- 510(k) Number
- K001808 FDA UDI
- FDA Product Code
- HBL FDA UDI
- EMDN Code
- Z12109080 VARIOUS NEUROLOGY AND NEUROSURGERY INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED
- GMDN Term
- Surgical retraction system, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 882.4460 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Orthopaedic trocar blade, reusable
DORO COBRA® Quick-Clamp for Radiolucent Quick-Rail® by Black Forest Medical GmbH — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID
Similar devices
Also classified as Orthopaedic trocar blade, reusable.
- Trauma Fixation Systems — Biomet Orthopedics, Inc. · Class I
- LEVEL ONE TRANSBUCCAL — KLS-Martin L.P. · Class I
- Strauss Surgical — AMERICAN MEDICAL ENDOSCOPY · Class I
- Adapterkabel Touchproof für ALM Tube — inomed Medizintechnik GmbH · Class I
- EBA ONE — Citieffe · Class II
- Tympanon-Elektrode mit 1, 5mm Sicherheitsstecker — inomed Medizintechnik GmbH · Class I
- ARTHROLUTION — Richard Wolf GmbH · Class I
- Strauss Surgical — AMERICAN MEDICAL ENDOSCOPY · Class I
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 42504355PA04EP | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Black Forest Medical GmbH
- EUDAMED SRN
- DE-MF-000005752
Sources (2)
- EUDAMED 6c0ce0bf-5fd3-4111-af1f-f6283391d0ac 61 fields · synced Jul 11, 2026
- FDA UDI 21609e56-d995-4d37-9dbb-2b3f39f022d3 34 fields · synced May 30, 2026