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Volk Viva

FDA UDI

Class II (US FDA UDI)

by Volk Optical Inc.

Identity

Trade Name
Volk Viva FDA UDI
Generic Name
Ophthalmic fundus camera FDA UDI
Model / Reference
VVIVA1A FDA UDI

Identifiers

Primary DI / UDI-DI
00811608014708 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

Yes

FDA UDI

Category: Ophthalmic fundus camera

Volk Viva by Volk Optical 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

Manufacturer
Volk Optical Inc.

Sources (1)

  • FDA UDI ab7f2cc5-6b30-4b23-9c0f-300722a31f11 33 fields · synced Jun 6, 2026