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Lazic 74.362.45

by Peter Lazic GmbH

Lazic 74.362.45 is a Class I device made by Peter Lazic GmbH, listed in FDA GUDID since 20 Nov 2024 (UDI-DI 04250603749233), 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 Number04250603749233 UDI-DI Date20 Nov 2024ListedStatusListed 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  • Withdrawn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
Open-surgery biopsy forceps, reusable
Model / reference
74.362.45
Primary DI / UDI-DI
04250603749233
FDA product code
KAE
GMDN term
Open-surgery biopsy forceps, reusable
Device class
Class I
Regulation number
874.4420
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Open-surgery biopsy forceps, reusable

Similar devices

Other devices filed under FDA product code KAE (Forceps, Ent).

Other devices from Peter Lazic GmbH

See all devices from Peter Lazic GmbH →

Properties

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