Mirabor-Ca (12 Burs)- 355234

by Hager Worldwide, 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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	NumberD2483552340 UDI-DI	Date4 Aug 2023Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Mirabor-Ca (12 Burs)-
Generic name: Device sterilization/disinfection container, reusable
Model / reference: 355234

Primary DI / UDI-DI: D2483552340
FDA product code: NRD
GMDN term: Device sterilization/disinfection container, reusable

Device class: Class I
Regulation number: 872.6640
GUDID distribution status: In Commercial Distribution

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Properties

Premarket exempt

Other properties (14)

Supplied sterile: No
Sterilise before use: No
Single use: No
Implantable: No
Contains latex: No
Prescription use: No
Over-the-counter: No
Convenience kit: No
Combination product: No
HCT/P: No
Lot / batch number: No
Serial number: No
Expiration date: No
Manufacturing date: No