Identity
- Trade Name
- JEDMED FDA UDI
- Generic Name
- Ophthalmic examination slit lamp FDA UDI
- Device Name
- SLIT LAMP LENS F/HORUS SERIES 2 FDA UDI
- Model / Reference
- 39-7433-2 FDA UDI
- Description
- SLIT LAMP LENS F/HORUS SERIES 2 FDA UDI
Identifiers
- Catalog Number
- 39-7433-2 FDA UDI
- Primary DI / UDI-DI
- M63339743320 FDA UDI
- 510(k) Number
- K170470 FDA UDI
- FDA Product Code
- HJO FDA UDI
- GMDN Term
- Ophthalmic examination slit lamp FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.1850 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Ophthalmic examination slit lamp
Jedmed by JEDMED Instrument Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K170470 also covers:
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
- JEDMED Instrument Company
Sources (1)
- FDA UDI 2ec8b53a-274e-420d-bd02-70669b25631a 35 fields · synced Jun 8, 2026