Identity
- Trade Name
- GREENLIGHT FDA UDI
- Generic Name
- Endoscope sheath, reusable FDA UDI
- Device Name
- INNER SHEATH LASER THERAPY color code yellow, SL 235mm, oval, working channel for instruments up to 7Fr, slanted distal end, stainless steel, continuous irrigation, compatible with outer sheath 8632024, and telescopes Ø 4mm, 12°/30°, bayonet-cap, reusable FDA UDI
- Model / Reference
- 8632025 FDA UDI
- Description
- INNER SHEATH LASER THERAPY color code yellow, SL 235mm, oval, working channel for instruments up to 7Fr, slanted distal end, stainless steel, continuous irrigation, compatible with outer sheath 8632024, and telescopes Ø 4mm, 12°/30°, bayonet-cap, reusable FDA UDI
Identifiers
- Catalog Number
- 8632.025 FDA UDI
- Primary DI / UDI-DI
- 04055207018095 FDA UDI
- FDA Product Code
- FBO FDA UDI
- GMDN Term
- Endoscope sheath, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Greenlight by Richard Wolf GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Richard Wolf GmbH
Sources (1)
- FDA UDI 83d2bbed-02b8-4c22-a672-208e6c5f9ead 36 fields · synced May 30, 2026