Na 2410-29

by Zimmer, Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00889024062184 UDI-DI	Date9 May 2017Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic Name: Orthopaedic prosthesis implantation positioning instrument, reusable
Model / Ref / Catalog: 2410-29, 00-2410-029-00

Primary DI / UDI-DI: 00889024062184
FDA Product Code: HWE
GMDN Term: Orthopaedic prosthesis implantation positioning instrument, reusable

Device Class: Class I
Regulation Number: 878.4820
GUDID distribution status: In Commercial Distribution

Sterilization Method: Moist Heat or Steam Sterilization

Size: Length — 19.5 Centimeter

Other devices from Zimmer, Inc.

IDENTITY Humeral 120001790

Class I
IDENTITY Humeral 120001792

Class I
IDENTITY Humeral 120001791

Class I
IDENTITY Humeral 120001795

Class I
IDENTITY Humeral 120001793

Class I
Comprehensive Humeral 120001798

Class I

See all devices from Zimmer, Inc. →

Properties

Prescription Use
Premarket Exempt
Lot / Batch Number

Other properties (11)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Serial Number: No
Expiration Date: No
Manufacturing Date: No