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Verily Retinal Camera

FDA UDI

Class II (US FDA UDI)

by Verily Life Sciences, LLC

Identity

Trade Name
Verily Retinal Camera FDA UDI
Generic Name
Ophthalmic fundus camera FDA UDI
Device Name
The Verily Retinal Camera is an ophthalmic camera used to acquire and transmit digital images of the human eye, including the retina. It is a prescription-use only medical device. FDA UDI
Model / Reference
VRC-100 FDA UDI
Description
The Verily Retinal Camera is an ophthalmic camera used to acquire and transmit digital images of the human eye, including the retina. It is a prescription-use only medical device. FDA UDI

Identifiers

Primary DI / UDI-DI
10860000249543 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

Verily Retinal Camera by Verily Life Sciences, LLC — 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 5ad7e2b4-0ff9-4c10-acad-315ed53aa980 34 fields · synced May 30, 2026