Lazic

FDA UDI

Class II (US FDA UDI)

by Peter Lazic GmbH

Identity

Trade Name: LAZIC FDA UDI
Generic Name: Aneurysm clip applier FDA UDI
Device Name: D-CLIP APPLIER/ REMOVER, STANDARD/ MINI, UP ANGLED, 110 MM WORKING LENGTH, DOUBLE ACTION, BAYONET, VARIABLE JAW, 230 MM FDA UDI
Model / Reference: 35.427 FDA UDI
Description: D-CLIP APPLIER/ REMOVER, STANDARD/ MINI, UP ANGLED, 110 MM WORKING LENGTH, DOUBLE ACTION, BAYONET, VARIABLE JAW, 230 MM FDA UDI

Identifiers

Catalog Number: 35.427 FDA UDI
Primary DI / UDI-DI: 04250603744603 FDA UDI
FDA Product Code: HCI FDA UDI
GMDN Term: Aneurysm clip applier FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 882.4175 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

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Aneurysm clip applier

Lazic by Peter Lazic 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: Peter Lazic GmbH

Sources (1)

FDA UDI 012aedf6-657c-4a2b-8cdb-1a9f8efef30a 35 fields · synced May 31, 2026