VitreQ

FDA UDI

Class II (US FDA UDI)

by Vitreq B.V.

Identity

Trade Name: VitreQ FDA UDI
Generic Name: Ophthalmic laser system beam guide FDA UDI
Device Name: 23G 90° Directional Laser Probes, Iridex® Compatible FDA UDI
Model / Reference: LP23.I04 FDA UDI
Description: 23G 90° Directional Laser Probes, Iridex® Compatible FDA UDI

Identifiers

Primary DI / UDI-DI: 08719214222383 FDA UDI
FDA Product Code: HQF FDA UDI
HQB FDA UDI
GMDN Term: Ophthalmic laser system beam guide FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 886.4390 FDA UDI
886.4690 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Ophthalmic laser system beam guide

VitreQ by Vitreq B.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic laser system beam guide.

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25ga Stiff Illuminated MultiFlex™ Extendable Laser Probe, Iridex Connector — KATALYST SURGICAL, LLC · Class II
Synergetics — SYNERGETICS USA, INC. · Class II
23-27G BriteLight™ Angled 45° EndoProbe® Box of 6 — Iridex Corporation · Class II
OtoProbe™ Long Angled Single — Iridex Corporation · Class II
Synergetics — SYNERGETICS USA, INC. · Class II
OtoProbe™ Short Angled Box of 6 — Iridex Corporation · 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

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Manufacturer

Manufacturer: Vitreq B.V.

Sources (1)

FDA UDI 31fd216b-25d1-4e77-a6b3-a6a797366d00 34 fields · synced May 30, 2026