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Auto Lensmeter

FDA UDIEUDAMED

Class I (US FDA UDI)

by View-M Technology Co., Ltd.

Identity

Trade Name
Auto Lensmeter FDA UDI
Generic Name
Manually-adjusted lensmeter, line-powered FDA UDI
Device Name
This device aims to take the measurements of vertex powers, cylinder axis, prismatic power and prism base setting within a restricted area of unprocessed lens, processed framed lens and contact lens, Auto Lensmeter also has functions to measure UV/BLUE transmission. As an external feature, the angle of the LCD can be changed. User is able to measure the PD and OH value with the horizontal and vertical ruler GUI after adjusting the extended LCD at the lowest angle. FDA UDI
Model / Reference
ALM-1P FDA UDI
Description
This device aims to take the measurements of vertex powers, cylinder axis, prismatic power and prism base setting within a restricted area of unprocessed lens, processed framed lens and contact lens, Auto Lensmeter also has functions to measure UV/BLUE transmission. As an external feature, the angle of the LCD can be changed. User is able to measure the PD and OH value with the horizontal and vertical ruler GUI after adjusting the extended LCD at the lowest angle. FDA UDI

Identifiers

Catalog Number
ALM-1P FDA UDI
Primary DI / UDI-DI
08800074500251 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 by View-M Technology Co., Ltd. — Class I — MDD, MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Manually-adjusted lensmeter, line-powered.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI f842d712-01b5-4754-904e-de2f344406dc 36 fields · synced Jun 19, 2026
  • EUDAMED 1 fields · synced Jun 2, 2026