Trident 2121 R 20 Cs

Trident 2121 R 20 Cs is a Class II device made by Technix SpA, listed in FDA GUDID since 6 Nov 2024 (UDI-DI 08053307591070), 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	Number08053307591070 UDI-DI	Date6 Nov 2024Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 08053307591070

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Trident
Generic name: Mobile general-purpose fluoroscopic x-ray system, digital
Model / reference: 2121 R 20 CS
Description: Mobile equipment for radioscopy and radiography Brand: Dornier MedTech America, Inc

Primary DI / UDI-DI: 08053307591070
FDA product code: JAA, OWB, OXO
GMDN term: Mobile general-purpose fluoroscopic x-ray system, digital

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

Similar devices in this category

Other devices filed under Mobile general-purpose fluoroscopic x-ray system, digital.

Other devices from Technix SpA

Nautilus

Class II
Trident 3030 R 20 Cs

Class II

Properties

Serial number
Manufacturing date

Other properties (13, all answered No)