Medtronic Reusable Instruments CDS2A

by Medtronic Sofamor Danek, Inc.

Medtronic Reusable Instruments CDS2A is a Class I device made by Medtronic Sofamor Danek, Inc., listed in FDA GUDID since 15 Oct 2022 (UDI-DI 00643169100749), 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	Number00643169100749 UDI-DI	Date15 Oct 2022Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00643169100749

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Medtronic Reusable Instruments
Generic name: Orthopaedic implantable material dispenser, reservoir-containing
Model / reference: CDS2A

Primary DI / UDI-DI: 00643169100749
FDA product code: KIH
GMDN term: Orthopaedic implantable material dispenser, reservoir-containing

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

Other devices from Medtronic Sofamor Danek, Inc.

MSB Reusable Instruments 9870005

Class I
MSB CD HORIZON Spinal System 6530530

Class II
T2 STRATOSPHERE™ Expandable Corpectomy System 436125C

Class II
MSB SHILLA Growth Guidance System 7670431

Class II

See all devices from Medtronic Sofamor Danek, Inc. →

Properties

Supplied sterile
Single use
Premarket exempt
Lot / batch number

Other properties (11, all answered No)