SEDECAL PhoeniX

by Sedecal., Sa. 12 variants

SEDECAL PhoeniX (4632) is a Class II device made by Sedecal., Sa., listed in FDA GUDID since 27 Sep 2021 (UDI-DI 08436046002999), not in commercial distribution (GUDID) as of 23 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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	Number08436046002999 UDI-DI	Date27 Sep 2021Listed	StatusListed GUDID: not in commercial distribution

Official records

AccessGUDID record UDI-DI 08436046002999

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Sedecal
Generic name: Mobile basic diagnostic x-ray system, digital
Model / Ref / Catalog: PhoeniX, 4632

Primary DI / UDI-DI: 08436046002999
FDA product code: MQB, IZL
GMDN term: Mobile basic diagnostic x-ray system, digital

Device class: Class II
Regulation number: 892.1680, 892.1720
GUDID distribution status: Not in Commercial Distribution

Similar devices in this category

Other devices filed under Mobile basic diagnostic x-ray system, digital.

Other devices from Sedecal., Sa.

Sedecal Net 4000-St

Class II
Sedecal SHFR400

Class I
MobileDiagnost wDR 2.2 Open recall

Class II
Sedecal Sm-40HF-B-D-C Open recall

Class II

See all devices from Sedecal., Sa. →

Properties

Prescription use
Serial number
Manufacturing date

Other properties (12, all answered No)