← Back to catalogue

Remidio

FDA UDI

Class I (US FDA UDI)

by Remidio Innovative Solutions Private Limited

Identity

Trade Name
Remidio FDA UDI
Generic Name
Automated ophthalmic refractometer FDA UDI
Device Name
The Auto ref/keratometer is used to measure the spherical, cylinder, axial, PD, corneal radius and corneal diopter of the patient's eye. FDA UDI
Model / Reference
REM-900 FDA UDI
Description
The Auto ref/keratometer is used to measure the spherical, cylinder, axial, PD, corneal radius and corneal diopter of the patient's eye. FDA UDI

Identifiers

Catalog Number
1010010005 FDA UDI
Primary DI / UDI-DI
08906096520083 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

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Automated ophthalmic refractometer

Remidio by Remidio Innovative Solutions Private Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Automated ophthalmic refractometer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 2da75ca6-5dd9-4617-b30c-89a77b562e09 35 fields · synced Jun 8, 2026