Profess

FDA UDI

Class II (US FDA UDI)

by Stryker Leibinger

Identity

Trade Name: PROFESS FDA UDI
Generic Name: Stereotactic surgery system probe, single-use FDA UDI
Device Name: PROFESS(TM) STRAIGHT SUCTION FDA UDI
Model / Reference: 6001-410-000 FDA UDI
Description: PROFESS(TM) STRAIGHT SUCTION FDA UDI

Identifiers

Catalog Number: 6001-410-000 FDA UDI
Primary DI / UDI-DI: 07613252727019 FDA UDI
FDA Product Code: PGW FDA UDI
GMDN Term: Stereotactic surgery system probe, single-use 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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Stereotactic surgery system probe, single-use

Profess by Stryker Leibinger — 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: Stryker Leibinger

Sources (1)

FDA UDI 391df6b4-e439-4694-9c00-ad104b4cf038 35 fields · synced May 30, 2026