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Disposable Vein Hook

FDA UDI

Class I (US FDA UDI)

by Vascular Solutions, Inc.

Identity

Trade Name
Disposable Vein Hook FDA UDI
Generic Name
Vein stripper, single-use FDA UDI
Device Name
The Disposable Vein Hook is intended for single patient use for the treatment of superficial varicose veins and varicosities associated with superficial reflux and incompetence of the Great Saphenous Vein in the lower extremities. FDA UDI
Model / Reference
7800 FDA UDI
Description
The Disposable Vein Hook is intended for single patient use for the treatment of superficial varicose veins and varicosities associated with superficial reflux and incompetence of the Great Saphenous Vein in the lower extremities. FDA UDI

Identifiers

Primary DI / UDI-DI
M20678000 FDA UDI
FDA Product Code
GAJ FDA UDI
GMDN Term
Vein stripper, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Disposable Vein Hook by Vascular Solutions, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c7e34410-3f3b-4ee0-8b93-5855cdacf370 35 fields · synced May 30, 2026