Landanger O614019

Landanger O614019 is a Class I device made by Landanger, listed in FDA GUDID since 17 Feb 2025 (UDI-DI 03661219268468), registry data as of 22 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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number03661219268468 UDI-DI	Date17 Feb 2025Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 03661219268468

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Landanger
Generic name: Surgical instrument interim-placement holder, reusable
Model / reference: O614019

Primary DI / UDI-DI: 03661219268468
FDA product code: LRP
GMDN term: Surgical instrument interim-placement holder, reusable

Device class: Class I
Regulation number: 878.4800
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

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Properties

Sterilise before use
Premarket exempt
Lot / batch number

Other properties (12, all answered No)