6550042

by Medtronic Sofamor Danek, Inc.

6550042 is a Class I device made by Medtronic Sofamor Danek, Inc., listed in FDA GUDID since 28 Dec 2024 (UDI-DI 00763000711993), registry data as of 9 Nov 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 9 Nov 2026.

Regulatory status

as of registry sync 9 Nov 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00763000711993 UDI-DI	Date28 Dec 2024Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00763000711993

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic name: Orthopaedic implantable material dispenser, cartridge-/syringe-accepting, reusable
Model / reference: 6550042

Primary DI / UDI-DI: 00763000711993
FDA product code: KIH
GMDN term: Orthopaedic implantable material dispenser, cartridge-/syringe-accepting, reusable

Device class: Class I
Regulation number: 888.4200
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

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Properties

Sterilise before use
Prescription use
Premarket exempt
Lot / batch number

Other properties (11, all answered No)