Lazic

FDA UDI

Class I (US FDA UDI)

by Peter Lazic GmbH

Identity

Trade Name: LAZIC FDA UDI
Generic Name: Neurosurgical scissors FDA UDI
Device Name: CLASSIC MICRO SCISSORS BAYONET CURVED, WORKING LENGTH 90 MM / 3 1/2" JAWS: SHARP, BLACK FDA UDI
Model / Reference: 70.023.04 B FDA UDI
Description: CLASSIC MICRO SCISSORS BAYONET CURVED, WORKING LENGTH 90 MM / 3 1/2" JAWS: SHARP, BLACK FDA UDI

Identifiers

Catalog Number: 70.023.04 B FDA UDI
Primary DI / UDI-DI: 04250603744917 FDA UDI
FDA Product Code: LRW FDA UDI
GMDN Term: Neurosurgical scissors FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Neurosurgical scissors

Lazic by Peter Lazic GmbH — Class I — 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 I	Pending data

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Manufacturer

Manufacturer: Peter Lazic GmbH

Sources (1)

FDA UDI cc1afd2a-6354-4c09-a8f6-9ce620d4f6e8 35 fields · synced Jun 8, 2026