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DORO® Transitional Member RDL (to ALU Base Unit)
EUDAMEDFDA UDIClass I (EU MDR)
Ref 3032-00
Identity
- Trade Name
- DORO® Transitional Member RDL (to ALU Base Unit) EUDAMEDDORO® Transitional Member FDA UDI
- Generic Name
- Skull clamp FDA UDI
- Device Name
- Headrestsystem Imaging EUDAMEDDORO® Transitional Member RDL (to ALU Base Unit) FDA UDI
- Model / Reference
- 3032-00 EUDAMEDFDA UDI
- Description
- DORO® Transitional Member RDL (to ALU Base Unit) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04250435502006 EUDAMEDFDA UDI
- Basic UDI-DI
- 42504355PA01EH EUDAMED
- Direct Marketing DI
- 04250435502006 EUDAMED
- 510(k) Number
- K032331 FDA UDI
- FDA Product Code
- HBL FDA UDI
- EMDN Code
- Z12109080 VARIOUS NEUROLOGY AND NEUROSURGERY INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED
- GMDN Term
- Skull clamp 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
Category: Orthopaedic trocar blade, reusable
DORO® Transitional Member RDL (to ALU Base Unit) by Black Forest Medical GmbH — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID
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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 | 42504355PA01EH | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Black Forest Medical GmbH
- EUDAMED SRN
- DE-MF-000005752
Sources (2)
- EUDAMED a2cfa2dc-26aa-4e6b-871e-53649abc5637 61 fields · synced Jul 17, 2026
- FDA UDI cf50a72e-7733-4399-8f77-b6182b5405c9 34 fields · synced May 29, 2026