← Back to catalogue

Symphony™

FDA UDI

Class II (US FDA UDI)

by Qfix

Identity

Trade Name
Symphony™ FDA UDI
Generic Name
Patient lifting system stretcher FDA UDI
Device Name
Symphony™ Brachytherapy Transfer Device with Cutout FDA UDI
Model / Reference
RT-5100-06 FDA UDI
Description
Symphony™ Brachytherapy Transfer Device with Cutout FDA UDI

Identifiers

Catalog Number
RT-5100-06 FDA UDI
Primary DI / UDI-DI
10841962110713 FDA UDI
FDA Product Code
OUO FDA UDI
LHN FDA UDI
LNH FDA UDI
KPS FDA UDI
JAK FDA UDI
IYE FDA UDI
JAI FDA UDI
FRZ FDA UDI
GMDN Term
Patient lifting system stretcher FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1200 FDA UDI
892.5050 FDA UDI
892.1000 FDA UDI
892.1750 FDA UDI
892.5770 FDA UDI
880.6775 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Patient lifting system stretcher

Symphony™ by Qfix — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient lifting system stretcher.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Qfix

Sources (1)

  • FDA UDI 35d19685-0bfc-4ea3-8e73-e71ce2ed9c1e 35 fields · synced Jun 8, 2026