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Vitalitec

FDA UDI

Class II (US FDA UDI)

by Vitalitec International Medizintechnik GmbH

Identity

Trade Name
Vitalitec FDA UDI
Generic Name
Spinal rongeur FDA UDI
Device Name
QUICK RELEASE Micro Kerrison Rongeur, micro thin footplate, 12 mm bite opening 40d UP, 2 mm, 12" FDA UDI
Model / Reference
VK.J1202QR FDA UDI
Description
QUICK RELEASE Micro Kerrison Rongeur, micro thin footplate, 12 mm bite opening 40d UP, 2 mm, 12" FDA UDI

Identifiers

Catalog Number
VK.J1202QR FDA UDI
Primary DI / UDI-DI
04250325494886 FDA UDI
FDA Product Code
HAE FDA UDI
GMDN Term
Spinal rongeur 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Spinal rongeur

Vitalitec by Vitalitec International Medizintechnik GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal rongeur.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vitalitec International Medizintechnik GmbH

Sources (1)

  • FDA UDI 2bb27ca2-f7b5-4f4d-930a-2c1ca44830d0 34 fields · synced May 30, 2026