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Arthroscopic sheaths
EUDAMEDFDA UDIClass I (EU MDR)
Ref 89220.1408Model 10000201091
Identity
- Trade Name
- VERTEBRIS FDA UDI
- Generic Name
- Endoscope sheath, reusable FDA UDI
- Device Name
- Arthroscopic sheaths EUDAMEDEXTENSION SLEEVE ID 7MM OD 8MM TL 155mm, distal end straight, reusable FDA UDI
- Model / Reference
- 10000201091 EUDAMED89220.1408 EUDAMED892201408 FDA UDI
- Description
- EXTENSION SLEEVE ID 7MM OD 8MM TL 155mm, distal end straight, reusable FDA UDI
Identifiers
- Catalog Number
- 89220.1408 FDA UDI
- Primary DI / UDI-DI
- 04055207046845 EUDAMEDFDA UDI
- Basic UDI-DI
- 405520720052019-0017663DG EUDAMED
- Direct Marketing DI
- 04055207046845 EUDAMED
- FDA Product Code
- NBH FDA UDI
- EMDN Code
- Z12021199 ORTHOPAEDIC ENDOSCOPY INSTRUMENTS - OTHER EUDAMED
- GMDN Term
- Endoscope sheath, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 888.1100 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
No
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Length — 154.6 Millimeter FDA UDIOuter Diameter — 8 Millimeter FDA UDILumen/Inner Diameter — 7 Millimeter FDA UDI
Arthroscopic sheaths by Richard Wolf GmbH — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
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 | 405520720052019-0017663DG | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Richard Wolf GmbH
- EUDAMED SRN
- DE-MF-000007048
Sources (2)
- EUDAMED 47804ec1-9590-44c8-9729-657e2f562e15 61 fields · synced Jun 18, 2026
- FDA UDI a2185e59-f5fe-4524-8a24-d33e3ca71425 36 fields · synced May 22, 2026