← Back to catalogue

IMAGEnet 5 OPHTHALMIC DATA SYSTEM

FDA UDI

Class II (US FDA UDI)

by Topcon Corp.

Identity

Trade Name
IMAGEnet 5 OPHTHALMIC DATA SYSTEM FDA UDI
Generic Name
Camera application software FDA UDI
Model / Reference
IMAGEnet 5 FDA UDI

Identifiers

Primary DI / UDI-DI
04562123288308 FDA UDI
FDA Product Code
NFJ FDA UDI
GMDN Term
Camera application software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.2050 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Camera application software

IMAGEnet 5 OPHTHALMIC DATA SYSTEM by Topcon Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Camera application software.

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

Manufacturer
Topcon Corp.

Sources (1)

  • FDA UDI c6cc1c7e-945b-4082-b2de-835c9b9a26f0 32 fields · synced May 30, 2026