Peripheral Vascular Sheath Tunneler

FDA UDI

Class II (US FDA UDI)

by Bard Peripheral Vascular

Identity

Trade Name: Peripheral Vascular Sheath Tunneler FDA UDI
Generic Name: Vascular graft tunneller FDA UDI
Device Name: Peripheral Vascular Sheath Tunneler FDA UDI
Model / Reference: PVT2000 FDA UDI
Description: Peripheral Vascular Sheath Tunneler FDA UDI

Identifiers

Catalog Number: PVT2000 FDA UDI
Primary DI / UDI-DI: 00801741132162 FDA UDI
FDA Product Code: MZY FDA UDI
GMDN Term: Vascular graft tunneller FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.3450 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Vascular graft tunneller

Peripheral Vascular Sheath Tunneler by Bard Peripheral Vascular — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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 II	Pending data

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Manufacturer

Manufacturer: Bard Peripheral Vascular

Sources (1)

FDA UDI 0ee3b891-0ea6-4aac-986e-2ffeb4210025 35 fields · synced May 31, 2026