Identity
- Trade Name
- Clement Clarke Ophthalmic FDA UDI
- Generic Name
- Ophthalmic binocular gauge FDA UDI
- Device Name
- RAF BINOCULAR GAUGE FDA UDI
- Model / Reference
- 7006001 FDA UDI
- Description
- RAF BINOCULAR GAUGE FDA UDI
Identifiers
- Catalog Number
- 7006001 FDA UDI
- Primary DI / UDI-DI
- 05060179470375 FDA UDI
- FDA Product Code
- HLE FDA UDI
- GMDN Term
- Ophthalmic binocular gauge FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.1790 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Ophthalmic binocular gauge
Clement Clarke Ophthalmic by Haag-Streit Uk Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Ophthalmic binocular gauge.
- Brock String — Gulden Ophthalmics · 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 I | Pending data |
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Manufacturer
- Manufacturer
- Haag-Streit Uk Limited
Sources (1)
- FDA UDI aa02e6ee-27f9-4c80-8ef9-bf0c288b00c6 35 fields · synced May 30, 2026