Identity
- Trade Name
- LIGHT GUIDE FDA UDI
- Generic Name
- Endoscopic light source adaptor FDA UDI
- Device Name
- LT GUIDE GEMINI 5MM X 10FT FDA UDI
- Model / Reference
- 7205178 FDA UDI
- Description
- LT GUIDE GEMINI 5MM X 10FT FDA UDI
Identifiers
- Catalog Number
- 7205178 FDA UDI
- Primary DI / UDI-DI
- 03596010373236 FDA UDI
- 510(k) Number
- K914919 FDA UDI
- FDA Product Code
- GCJ 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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Endoscopic light source adaptor
Light Guide by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K914919 also covers:
- GEMINI — Smith & Nephew, Inc.
- GEMINI — Smith & Nephew, Inc.
- GEMINI — Smith & Nephew, Inc.
- GEMINI — Smith & Nephew, Inc.
- GEMINI — Smith & Nephew, Inc.
- GEMINI — Smith & Nephew, Inc.
- LIGHT GUIDE — Smith & Nephew, Inc.
- STORZ — Smith & Nephew, Inc.
- VERSITIP — Smith & Nephew, Inc.
- VERSITIP — Smith & Nephew, Inc.
- VERSITIP — Smith & Nephew, Inc.
- VERSITIP — Smith & Nephew, Inc.
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Smith & Nephew, Inc.
Sources (1)
- FDA UDI 163a0b23-d4a7-45e6-9a56-18ec1d6efde2 36 fields · synced Jun 8, 2026