Symphony™ RT-5100-06

Symphony™ RT-5100-06 is a Class II device made by Qfix, listed in FDA GUDID since 18 Apr 2018 (UDI-DI 10841962110713), 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	Number10841962110713 UDI-DI	Date18 Apr 2018Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 10841962110713

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Symphony™
Generic name: Patient lifting system stretcher
Model / Ref / Catalog: RT-5100-06

Primary DI / UDI-DI: 10841962110713
FDA product code: OUO, LHN, LNH, KPS, JAK, IYE, JAI, FRZ
GMDN term: Patient lifting system stretcher

Device class: Class II
Regulation number: 892.1200, 892.5050, 892.1000, 892.1750, 892.5770, 880.6775
GUDID distribution status: In Commercial Distribution

MRI safety: MR Conditional

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Properties

Prescription use
Serial number
Manufacturing date

Other properties (12, all answered No)