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Lazic 46.144

by Peter Lazic GmbH

Lazic 46.144 is a Class I device made by Peter Lazic GmbH, listed in FDA GUDID since 30 Jul 2020 (UDI-DI 04250603712992), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04250603712992 UDI-DI Date30 Jul 2020ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Lazic
Generic name
Scalpel, reusable
Model / Ref / Catalog
46.144
Primary DI / UDI-DI
04250603712992
FDA product code
EMF
GMDN term
Scalpel, reusable
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Scalpel, reusable

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Other devices filed under Scalpel, reusable.

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)