Identity
- Trade Name
- LuxVsion FDA UDI
- Generic Name
- Phoropter, electric FDA UDI
- Device Name
- Luxvision Digital Refractor LDR-7800 FDA UDI
- Model / Reference
- LDR-7800 FDA UDI
- Description
- Luxvision Digital Refractor LDR-7800 FDA UDI
Identifiers
- Catalog Number
- LDR-7800 FDA UDI
- Primary DI / UDI-DI
- 00850038195557 FDA UDI
- FDA Product Code
- HKN FDA UDI
- GMDN Term
- Phoropter, electric FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.1770 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Phoropter, electric
LuxVsion by U.s. Ophthalmic, L.l.c. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- U.s. Ophthalmic, L.l.c.
Sources (1)
- FDA UDI 8d51c4f0-e9aa-4482-8997-e9d79f9ac7e6 34 fields · synced May 30, 2026