← Back to catalogue
Arthroscopic hammers
EUDAMEDFDA UDIClass I (EU MDR)
Ref 8866.956Model 10000201168
Identity
- Trade Name
- NA FDA UDI
- Generic Name
- Surgical mallet FDA UDI
- Device Name
- Arthroscopic hammers EUDAMEDACL HAMMER TL 248MM reusable FDA UDI
- Model / Reference
- 10000201168 EUDAMED8866.956 EUDAMED8866956 FDA UDI
- Description
- ACL HAMMER TL 248MM reusable FDA UDI
Identifiers
- Catalog Number
- 8866.956 FDA UDI
- Primary DI / UDI-DI
- 04055207021217 EUDAMEDFDA UDI
- Basic UDI-DI
- 405520722052019-0017831GB EUDAMED
- Direct Marketing DI
- 04055207021217 EUDAMED
- FDA Product Code
- FZY FDA UDI
- EMDN Code
- L0903 ORTHOPAEDIC SURGERY HAMMERS, REUSABLE EUDAMED
- GMDN Term
- Surgical mallet FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 878.4800 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 — 248 Millimeter FDA UDI
Arthroscopic hammers 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 | 405520722052019-0017831GB | 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
- Richard Wolf GmbH
- EUDAMED SRN
- DE-MF-000007048
Sources (2)
- EUDAMED d3b9198e-df4e-4f4c-86f8-fd76f7d99fda 61 fields · synced Jun 17, 2026
- FDA UDI a01e07f1-ebda-43b9-9281-d0ab2f2e0e29 36 fields · synced May 30, 2026