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Dr. Vampa

FDA UDI

Class I (US FDA UDI)

by Dr Vampa S.R.L.

Identity

Trade Name
Dr. Vampa FDA UDI
Generic Name
Mobile examination/treatment room light FDA UDI
Device Name
Portable, battery-powered LED light device designed to assist in the visualization of superficial veins by emitting orange light that enhances vein contrast through the skin. Ideal for use in medical settings to aid in vein location for procedures such as venipuncture and IV insertion. FDA UDI
Model / Reference
Veif Pro - Black FDA UDI
Description
Portable, battery-powered LED light device designed to assist in the visualization of superficial veins by emitting orange light that enhances vein contrast through the skin. Ideal for use in medical settings to aid in vein location for procedures such as venipuncture and IV insertion. FDA UDI

Identifiers

Catalog Number
XR 17090-BL FDA UDI
Primary DI / UDI-DI
07465850912010 FDA UDI
FDA Product Code
KYT FDA UDI
GMDN Term
Mobile examination/treatment room light FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6350 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

Yes

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

No

FDA UDI

Category: Mobile examination/treatment room light

Dr. Vampa by Dr Vampa S.R.L. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Mobile examination/treatment room light.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dr Vampa S.R.L.

Sources (1)

  • FDA UDI dd3e91c7-3e00-42ec-8221-36d1353ab5aa 36 fields · synced May 30, 2026