Identity
- Trade Name
- KR-1W Viewer FDA UDI
- Generic Name
- Automated ophthalmic refractometer FDA UDI
- Model / Reference
- KR-1W Viewer FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04560126266071 FDA UDI
- FDA Product Code
- HKO FDA UDI
- GMDN Term
- Automated ophthalmic refractometer FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.1760 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Automated ophthalmic refractometer
KR-1W Viewer by Topcon Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- AUTO REF/KERATO/TONOMETER — Nidek, Inc. · Class II
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
- Topcon Corp.
Sources (1)
- FDA UDI eb3c3275-56bc-41e5-ae9c-78af544b5bcb 32 fields · synced Jun 8, 2026