2358-2000

by Stryker Corp.

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	Number07613327346282 UDI-DI	Date13 Jul 2020Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic name: Manual surgical rotary handpiece, reusable
Model / Ref / Catalog: 2358-2000

Primary DI / UDI-DI: 07613327346282
FDA product code: HWE
GMDN term: Manual surgical rotary handpiece, reusable

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

Sterilisation method: Moist Heat or Steam Sterilization

Other devices from Stryker Corp.

Excelsior Reach MC17PSJ155-01

Class II
Excelsior Reach MC17PS90155-01

Class II
Excelsior Reach MC17PS45165-01

Class II
Excelsior Reach MC17ST155-01

Class II
Excelsior Reach MC17PS90165-01

Class II
Excelsior Reach MC17PS45155-01

Class II

See all devices from Stryker Corp. →

Properties

Sterilise before use
Prescription use
Premarket exempt
Lot / batch number

Other properties (11)

Supplied 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