Identity
- Trade Name
- ALM700 FDA UDI
- Generic Name
- Automated lensmeter FDA UDI
- Device Name
- This device aims to take the measurements of SPH, CYL, AXIS, prism refractive power and optical axis coordinate of unprocessed lens, processed framed lens and contact lens, and to put dots on them to find its axis FDA UDI
- Model / Reference
- ALM700 FDA UDI
- Description
- This device aims to take the measurements of SPH, CYL, AXIS, prism refractive power and optical axis coordinate of unprocessed lens, processed framed lens and contact lens, and to put dots on them to find its axis FDA UDI
Identifiers
- Primary DI / UDI-DI
- 03615020000120 FDA UDI
- FDA Product Code
- HLM FDA UDI
- GMDN Term
- Automated lensmeter 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: Automated lensmeter
Alm700 by Essilor International — 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
- Essilor International
Sources (1)
- FDA UDI 9ab4f028-ed1b-4ec2-be6f-4ac17b7a1323 35 fields · synced May 30, 2026