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Virtual Eye Software

FDA UDI

Class I (US FDA UDI)

by Virtual Vision Health

Identity

Trade Name
Virtual Eye Software FDA UDI
Generic Name
Perimeter, automatic FDA UDI
Model / Reference
3.2.0 FDA UDI

Identifiers

Catalog Number
VV-021 FDA UDI
Primary DI / UDI-DI
00860010709795 FDA UDI
FDA Product Code
HIT FDA UDI
HRI FDA UDI
HPT FDA UDI
GMDN Term
Perimeter, automatic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.1170 FDA UDI
886.1690 FDA UDI
886.1605 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Perimeter, automatic

Virtual Eye Software by Virtual Vision Health — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Perimeter, automatic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 70642e72-064d-4e33-9e3b-bd19cd823420 33 fields · synced Jun 8, 2026