Veritas Vision System

FDA UDI

Class II (US FDA UDI)

by Johnson & Johnson Surgical Vision, Inc.

Identity

Trade Name: VERITAS VISION SYSTEM FDA UDI
Generic Name: Phacoemulsification system FDA UDI
Device Name: VERITAS CONSOLE FDA UDI
Model / Reference: VRT680300 FDA UDI
Description: VERITAS CONSOLE FDA UDI

Identifiers

Catalog Number: VRT680300 FDA UDI
Primary DI / UDI-DI: 05050474700864 FDA UDI
FDA Product Code: HQC FDA UDI
GMDN Term: Phacoemulsification system FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 886.4670 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Phacoemulsification system

Veritas Vision System by Johnson & Johnson Surgical Vision, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Phacoemulsification system.

Operators Manual, M2000, Premium — MEDICAL TECHNICAL PRODUCTS, INC · Class II
Operators Manual, M2000, Value, Chinese — MEDICAL TECHNICAL PRODUCTS, INC · Class II
Operators Manual, M2000, Value — MEDICAL TECHNICAL PRODUCTS, INC · Class II
Console, M2000, Premium — MEDICAL TECHNICAL PRODUCTS, INC · Class II
Centurion — Alcon Laboratories, Inc. · Class II
Console, M2000, Value — MEDICAL TECHNICAL PRODUCTS, INC · Class II
Console, M2000, Enhanced — MEDICAL TECHNICAL PRODUCTS, INC · Class II
Operators Manual, M3000 — MEDICAL TECHNICAL PRODUCTS, INC · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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

Manufacturer

Manufacturer: Johnson & Johnson Surgical Vision, Inc.

Sources (1)

FDA UDI f77e73e2-708d-4ee0-8197-20a5b6e5952c 36 fields · synced Jun 9, 2026