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VF1000LED Vein locator

FDA UDI

Class I (US FDA UDI)

by Fabinject Industria E Comercio Importacao E Exportacao Ltda

Identity

Trade Name
VF1000LED Vein locator FDA UDI
Generic Name
Visible-light skin transilluminator FDA UDI
Device Name
A device designed to locate veins through cutaneous transillumination. FDA UDI
Model / Reference
VF1000LEDBX1 FDA UDI
Description
A device designed to locate veins through cutaneous transillumination. FDA UDI

Identifiers

Primary DI / UDI-DI
07898915128789 FDA UDI
FDA Product Code
HJN FDA UDI
GMDN Term
Visible-light skin transilluminator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.1945 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

No

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

Yes

FDA UDI

Category: Visible-light skin transilluminator

VF1000LED Vein locator by Fabinject Industria E Comercio Importacao E Exportacao Ltda — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Visible-light skin transilluminator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fabinject Industria E Comercio Importacao E Exportacao Ltda

Sources (1)

  • FDA UDI 604f7fc2-ad41-4e02-84ae-ba6f2073933a 34 fields · synced May 30, 2026