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VitreQ

FDA UDI

Class I (US FDA UDI)

by Vitreq B.V.

Identity

Trade Name
VitreQ FDA UDI
Generic Name
Vitrectomy fluid/gas handling handpiece/cannula FDA UDI
Device Name
25G Extendable Silicone Tipped BF-Instrument FDA UDI
Model / Reference
BF25.D07 FDA UDI
Description
25G Extendable Silicone Tipped BF-Instrument FDA UDI

Identifiers

Primary DI / UDI-DI
88719214220958 FDA UDI
FDA Product Code
HMX FDA UDI
GMDN Term
Vitrectomy fluid/gas handling handpiece/cannula FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Vitrectomy fluid/gas handling handpiece/cannula

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

Similar devices

Also classified as Vitrectomy fluid/gas handling handpiece/cannula.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vitreq B.V.

Sources (1)

  • FDA UDI 423f1313-d9bf-4ff3-ac4a-9cc2b9acc4af 34 fields · synced May 30, 2026