Identity
- Trade Name
- Finhoff Transilluminator 2.8v FDA UDI
- Generic Name
- Skin transilluminator, battery-powered FDA UDI
- Model / Reference
- 2903-P-1118 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05055272707794 FDA UDI
- FDA Product Code
- HJM FDA UDI
- GMDN Term
- Skin transilluminator, battery-powered FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.1945 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
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
Category: Skin transilluminator, battery-powered
Finhoff Transilluminator 2.8v by Keeler Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Skin transilluminator, battery-powered.
- SIMSYS — MedX Health Corp · Class II
- Venoscope — VENOSCOPE, LLC · Class I
- ASTODIA — Stihler Electronic GmbH · Class I
- MoleMate — MedX Health Corp · Class II
- Venoscope — VENOSCOPE, LLC · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Keeler Limited
Sources (1)
- FDA UDI d571baa4-0633-4578-bffe-569c0ed169ea 32 fields · synced Jun 8, 2026