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EyeSuite Software

FDA UDI

Class II (US FDA UDI)

by Haag-Streit AG

Identity

Trade Name
EyeSuite Software FDA UDI
Generic Name
Medical image management system FDA UDI
Model / Reference
i9.0 FDA UDI

Identifiers

Primary DI / UDI-DI
07640132987256 FDA UDI
FDA Product Code
NFJ FDA UDI
GMDN Term
Medical image management system 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

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Medical image management system

EyeSuite Software by Haag-Streit AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical image management system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Haag-Streit AG

Sources (1)

  • FDA UDI 5065b2ce-352d-431e-a659-981d3cd1aac8 33 fields · synced May 30, 2026