Identity
- Trade Name
- Universal Light Guide Adapter FDA UDI
- Generic Name
- Endoscopic light source adaptor FDA UDI
- Device Name
- MAJ-1200 CLV-S40 UNIVERSAL LIG HT GUIDE FDA UDI
- Model / Reference
- OLYMPUS MAJ-1200 FDA UDI
- Description
- MAJ-1200 CLV-S40 UNIVERSAL LIG HT GUIDE FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04953170155017 FDA UDI
- FDA Product Code
- FDS FDA UDI
- GMDN Term
- Endoscopic light source adaptor FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 FDA UDI
- Commercial Distribution
- 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
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Endoscopic light source adaptor
Universal Light Guide Adapter by Olympus Medical Systems Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Endoscopic light source adaptor.
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- FENTEX — FENTEX medical GmbH · Class I
- ACMI ADAPTOR — Biomet Orthopedics, Inc. · Class II
- Gimmi — Gimmi GmbH · Class II
- CONMED — Conmed Corporation · Class I
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
- Olympus Medical Systems Corporation
Sources (1)
- FDA UDI 684bfd67-f5f4-478b-9df0-77c8da9bf508 34 fields · synced Jun 1, 2026