Quick Release

FDA UDI

Class II (US FDA UDI)

by Vitalitec International Medizintechnik GmbH

Identity

Trade Name: Quick Release FDA UDI
Generic Name: Bone punch, reusable FDA UDI
Device Name: V-COAT bayoneted Kerrison, 1 mm, 40° 9" - quick release FDA UDI
Model / Reference: VK.J901CTBC FDA UDI
Description: V-COAT bayoneted Kerrison, 1 mm, 40° 9" - quick release FDA UDI

Identifiers

Catalog Number: VK.J901CTBC FDA UDI
Primary DI / UDI-DI: 04250325448728 FDA UDI
FDA Product Code: HAE FDA UDI
GMDN Term: Bone punch, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 882.4840 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

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Bone punch, reusable

Quick Release by Vitalitec International Medizintechnik GmbH — 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: Vitalitec International Medizintechnik GmbH

Sources (1)

FDA UDI 8f69e714-348f-4e59-b8fb-94944957eee9 34 fields · synced Jun 1, 2026