Carousel MAS1675-02

by Mazor Robotics Ltd

Carousel MAS1675-02 is a Class II device made by Mazor Robotics Ltd, listed in FDA GUDID since 22 Dec 2019 (UDI-DI 07290109182599), registry data as of 23 Oct 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number07290109182599 UDI-DI	Date22 Dec 2019Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 07290109182599

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Carousel
Generic name: Stereotactic surgery system probe, reusable
Model / reference: MAS1675-02

Primary DI / UDI-DI: 07290109182599
FDA product code: HAW, LLZ
GMDN term: Stereotactic surgery system probe, reusable

Device class: Class II
Regulation number: 882.4560, 892.2050
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

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Properties

Sterilise before use
Convenience kit
Lot / batch number
Serial number
Manufacturing date

Other properties (10, all answered No)