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Lazic

FDA UDI

Class I (US FDA UDI)

by Peter Lazic GmbH

Identity

Trade Name
LAZIC FDA UDI
Generic Name
Spinal rongeur FDA UDI
Device Name
KERRISON SWING PUNCH WITHOUT EJECTOR WIDTH OF BITE 2 MM, 40° THIN FOOTPLATE 15MM OPEN.W., SL 200 MM / 7 7/8", BLACK FDA UDI
Model / Reference
74.642.12 B FDA UDI
Description
KERRISON SWING PUNCH WITHOUT EJECTOR WIDTH OF BITE 2 MM, 40° THIN FOOTPLATE 15MM OPEN.W., SL 200 MM / 7 7/8", BLACK FDA UDI

Identifiers

Catalog Number
74.642.12 B FDA UDI
Primary DI / UDI-DI
04250603722083 FDA UDI
FDA Product Code
LRY FDA UDI
GMDN Term
Spinal rongeur 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Spinal rongeur

Lazic by Peter Lazic GmbH — Class I — 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
Peter Lazic GmbH

Sources (1)

  • FDA UDI 670274c8-3c64-4e9e-bc82-f81a631f12a1 35 fields · synced Jun 1, 2026