← Back to catalogue
Light cables for light sources
EUDAMEDFDA UDIClass I (EU MDR)
Ref 80662523Model 10000201043
Identity
- Trade Name
- FUSION-DESIGN FDA UDI
- Generic Name
- Fibreoptic light cable FDA UDI
- Device Name
- Light cables for light sources EUDAMEDFIBER LIGHT CABLE Ø 2.5MM TL 2.3M color code green FDA UDI
- Model / Reference
- 10000201043 EUDAMED80662523 EUDAMEDFDA UDI
- Description
- FIBER LIGHT CABLE Ø 2.5MM TL 2.3M color code green FDA UDI
Identifiers
- Catalog Number
- 80662523 FDA UDI
- Primary DI / UDI-DI
- 04055207026311 EUDAMEDFDA UDI
- Basic UDI-DI
- 405520711062019-0017590EH EUDAMED
- Direct Marketing DI
- 04055207026311 EUDAMED
- FDA Product Code
- FEM FDA UDI
- EMDN Code
- Z12020499 INSTRUMENTS FOR THE ACQUISITION AND MANAGEMENT OF ENDOSCOPIC AND MINIMALLY INVASIVE SURGERY IMAGES – OTHER EUDAMED
- GMDN Term
- Fibreoptic light cable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 876.1500 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- Not 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 — 2.3 Meter FDA UDIOuter Diameter — 2.5 Millimeter FDA UDI
Light cables for light sources 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 | 405520711062019-0017590EH | 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 2324f8aa-6de2-47bc-9eca-5bacd5be10e0 61 fields · synced Jul 18, 2026
- FDA UDI 5e46bc2c-ae95-474f-adac-812b49e39f94 37 fields · synced May 25, 2026