Identity
- Trade Name
- Auto Lensmeter HLM-7000 FDA UDI
- Generic Name
- Manually-adjusted lensmeter, line-powered FDA UDI
- Device Name
- Lensmeter is a machine to generate Sph, Cyl and Axis information of lens by measuring refraction of the lens FDA UDI
- Model / Reference
- HLM-7000 FDA UDI
- Description
- Lensmeter is a machine to generate Sph, Cyl and Axis information of lens by measuring refraction of the lens FDA UDI
Identifiers
- Catalog Number
- HLM-7000 FDA UDI
- Primary DI / UDI-DI
- 08800019600398 FDA UDI
- FDA Product Code
- HLM FDA UDI
- GMDN Term
- Manually-adjusted lensmeter, line-powered FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.1425 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: Manually-adjusted lensmeter, line-powered
Auto Lensmeter HLM-7000 by Huvitz Co., Ltd. — 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
- Huvitz Co., Ltd.
Sources (1)
- FDA UDI 26633322-1651-42d4-9145-fcc5b13dbf47 35 fields · synced May 30, 2026