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ResQUp

FDA UDI

Class I (US FDA UDI)

by Safe Patient Solutions, L.L.C.

Identity

Trade Name
ResQUp FDA UDI
Generic Name
Mobile patient lifting system, manual FDA UDI
Device Name
Self-Recovery device to assist a fallen person moving themselves to a seated position after a non-injurious fall. Color: Sea Salt FDA UDI
Model / Reference
Sea Salt FDA UDI
Description
Self-Recovery device to assist a fallen person moving themselves to a seated position after a non-injurious fall. Color: Sea Salt FDA UDI

Identifiers

Primary DI / UDI-DI
00860003643136 FDA UDI
FDA Product Code
IKX FDA UDI
GMDN Term
Mobile patient lifting system, manual FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5050 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

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Mobile patient lifting system, manual

ResQUp is a self-recovery device designed to assist individuals who have fallen and need assistance moving themselves to a seated position. This innovative product features a support base on wheels with a lifting mechanism, making it easy to lift and move patients or individuals with disabilities safely.

Similar devices

Also classified as Mobile patient lifting system, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ae02cc23-1f09-4ddd-a795-b3265f192c33 33 fields · synced Jun 29, 2026