Tischler Kevorkian Biopsy Punch

FDA UDI

Class I (US FDA UDI)

by Biopsy Fine Cut Instruments

Identity

Trade Name: TISCHLER KEVORKIAN BIOPSY PUNCH FDA UDI
Generic Name: Open-surgery biopsy forceps, reusable FDA UDI
Device Name: TISCHLER KEVORKIAN BIOPSY PUNCH 8.25" FDA UDI
Model / Reference: BP012 FDA UDI
Description: TISCHLER KEVORKIAN BIOPSY PUNCH 8.25" FDA UDI

Identifiers

Catalog Number: BP012 FDA UDI
Primary DI / UDI-DI: G422BP0120 FDA UDI
FDA Product Code: HFB FDA UDI
GMDN Term: Open-surgery biopsy forceps, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 884.4530 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

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

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Open-surgery biopsy forceps, reusable

Tischler Kevorkian Biopsy Punch by Biopsy Fine Cut Instruments — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Novo Surgical Inc. — NOVO SURGICAL, INC. · Class I

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 I	Pending data

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Manufacturer

Manufacturer: Biopsy Fine Cut Instruments

Sources (1)

FDA UDI b90bc208-6bab-4c02-8e68-a875661de2c3 34 fields · synced Jun 8, 2026