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Brainpro Stryker

FDA UDI

Class II (US FDA UDI)

by Pajunk GmbH Medizintechnologie

Identity

Trade Name
BRAINPRO STRYKER FDA UDI
Generic Name
Brain biopsy procedure kit FDA UDI
Device Name
6000-024-000 FDA UDI
Model / Reference
6000-024-000 FDA UDI
Description
6000-024-000 FDA UDI

Identifiers

Catalog Number
6000-024-000 FDA UDI
Primary DI / UDI-DI
04048223099384 FDA UDI
FDA Product Code
HAW FDA UDI
GMDN Term
Brain biopsy procedure kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4560 FDA UDI
Commercial Distribution
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

No

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Brain biopsy procedure kit

Brainpro Stryker by Pajunk GmbH Medizintechnologie — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Brain biopsy procedure kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1c29a4bc-9c75-481d-83fb-24e8df5fbb99 36 fields · synced May 30, 2026