← Back to catalogue

Welch Allyn

FDA UDI

Class II (US FDA UDI)

by Medimaging Integrated Solution Inc.

Identity

Trade Name
Welch Allyn FDA UDI
Generic Name
Ophthalmic fundus camera FDA UDI
Device Name
Eye Fundus Camera: RetinaVue 700 Imager (RV700B) FDA UDI
Model / Reference
1008 FDA UDI
Description
Eye Fundus Camera: RetinaVue 700 Imager (RV700B) FDA UDI

Identifiers

Primary DI / UDI-DI
04719872711131 FDA UDI
FDA Product Code
PJZ 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ophthalmic fundus camera

Welch Allyn by Medimaging Integrated Solution 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

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

Manufacturer

Sources (1)

  • FDA UDI cd796d43-caf8-4d1e-9679-1a1c98ecad91 33 fields · synced May 30, 2026