Identity
- Trade Name
- Symphony™ BoS™ FDA UDI
- Generic Name
- Patient lifting system stretcher FDA UDI
- Device Name
- Symphony™ Bos™ Transfer Device FDA UDI
- Model / Reference
- RT-5100-04 FDA UDI
- Description
- Symphony™ Bos™ Transfer Device FDA UDI
Identifiers
- Catalog Number
- RT-5100-04 FDA UDI
- Primary DI / UDI-DI
- 10841962110447 FDA UDI
- FDA Product Code
- KPS FDA UDIJAI FDA UDILNH FDA UDILHN FDA UDIFRZ FDA UDIIYE FDA UDIJAK FDA UDIOUO FDA UDI
- GMDN Term
- Patient lifting system stretcher FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.1200 FDA UDI892.5770 FDA UDI892.1000 FDA UDI892.5050 FDA UDI880.6775 FDA UDI892.1750 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
MR Safe FDA UDI
Category: Patient lifting system stretcher
Symphony™ BoS™ by Qfix — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Patient lifting system stretcher.
- Zephyr Patient Positioning and Transfer System — Diacor Inc. · Class I
- Zephyr Patient Positioning and Transfer System — Diacor Inc. · Class I
- Trans — Invacare GmbH · Class I
- Zephyr Patient Positioning and Transfer System — Diacor Inc. · Class I
- Transfer board — Mobilex A/S · Class I
- Powered Loading System (PLS) (Component) — LIFEPORT, LLC. · Class I
- INSTALLATION, POWER LOADING SYSTEM, CESSNA 680 * PLS — LIFEPORT, LLC. · Class I
- Zephyr Patient Positioning and Transfer System — Diacor Inc. · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Qfix
Sources (1)
- FDA UDI a315800d-4622-44a2-8f04-88d8bec7859a 36 fields · synced May 30, 2026