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Advancing Eyecare

FDA UDI

Class I (US FDA UDI)

by Lombart Brothers, Inc.

Identity

Trade Name
Advancing Eyecare FDA UDI
Generic Name
Phoropter, electric FDA UDI
Device Name
For checking the refractive state of human eye. FDA UDI
Model / Reference
RT-600 FDA UDI
Description
For checking the refractive state of human eye. FDA UDI

Identifiers

Primary DI / UDI-DI
00860014277504 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Phoropter, electric

Advancing Eyecare by Lombart Brothers, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Phoropter, electric.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 401f93bd-6db6-465c-931a-ce48d1598dec 33 fields · synced Jun 1, 2026