Vl

FDA UDI

Class III (US FDA UDI)

by BIOTRONIK SE & Co. KG

Identity

Trade Name: VL FDA UDI
Generic Name: Vein pick FDA UDI
Model / Reference: 106157 FDA UDI

Identifiers

Catalog Number: 106157 FDA UDI
Primary DI / UDI-DI: 04035479145293 FDA UDI
PMA Number: P980023 FDA UDI
FDA Product Code: DTB FDA UDI
GMDN Term: Vein pick FDA UDI

Classification

Device Class: Class III FDA UDI
Regulation Number: 870.3680 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: Vein pick

Vl by BIOTRONIK SE & Co. KG — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vein pick.

Wexler Surgical, Inc. — Wexler Surgical, Inc. · Class I
Vein Pick — Oscor Inc. · Class III
Vein Pick — Oscor Inc. · Class III

Cleared under the same submission

P980023 also covers:

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 III	Pending data

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Manufacturer

Manufacturer: BIOTRONIK SE & Co. KG

Sources (1)

FDA UDI 6577db3a-f4f4-4c12-b0c0-d08ebb09dead 35 fields · synced May 30, 2026