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Optina-4C

FDA UDI

Class II (US FDA UDI)

by Optina Diagnostiques, Inc

Identity

Trade Name
Optina-4C FDA UDI
Generic Name
Ophthalmic fundus camera FDA UDI
Device Name
Mydriatic Hyperspectral Retinal Camera (MHRC-C1N) FDA UDI
Model / Reference
MHRC-C1N FDA UDI
Description
Mydriatic Hyperspectral Retinal Camera (MHRC-C1N) FDA UDI

Identifiers

Primary DI / UDI-DI
00627987702132 FDA UDI
FDA Product Code
HKI FDA UDI
GMDN Term
Ophthalmic fundus camera FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.1120 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Ophthalmic fundus camera

Optina-4C by Optina Diagnostiques, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic fundus camera.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cec0dad0-c88a-4937-a1fa-4ca4fc144905 33 fields · synced Jun 8, 2026