Duet DRF 63111976

by Thales Avs France SAS

Duet DRF 63111976 is a Class II device made by Thales Avs France SAS, listed in FDA GUDID since 23 Oct 2020 (UDI-DI 03701440100035), 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	Number03701440100035 UDI-DI	Date23 Oct 2020Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 03701440100035

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Duet DRF
Generic name: Stationary general-purpose fluoroscopic x-ray system, digital
Model / reference: 63111976

Primary DI / UDI-DI: 03701440100035
FDA product code: JAA, MQB
GMDN term: Stationary general-purpose fluoroscopic x-ray system, digital

Device class: Class II
Regulation number: 892.1650, 892.1680
GUDID distribution status: In Commercial Distribution

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Properties

Serial number

Other properties (14, all answered No)