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Veritas Advanced Fluidics Pack

FDA UDI

Class II (US FDA UDI)

by Johnson & Johnson Surgical Vision, Inc.

Identity

Trade Name
VERITAS ADVANCED FLUIDICS PACK FDA UDI
Generic Name
Surgical irrigation/aspiration tubing set FDA UDI
Device Name
VERITAS ADVANCED FLUIDICS PACK FDA UDI
Model / Reference
VRT-AF FDA UDI
Description
VERITAS ADVANCED FLUIDICS PACK FDA UDI

Identifiers

Catalog Number
VRT-AF FDA UDI
Primary DI / UDI-DI
05050474700895 FDA UDI
FDA Product Code
HQC FDA UDI
GMDN Term
Surgical irrigation/aspiration tubing set 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

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical irrigation/aspiration tubing set

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

Similar devices

Also classified as Surgical irrigation/aspiration tubing set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 856ee2d6-48b7-415e-89a7-0846aaf81f61 35 fields · synced Jun 9, 2026