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Proactive

FDA UDI

Class I (US FDA UDI)

by Xiamen World Gear Sports Goods Co., Ltd

Identity

Trade Name
Proactive FDA UDI
Generic Name
Mobile patient lifting system, manual FDA UDI
Device Name
The Proactive Medical patient lift is intended to transfer an individual from one resting surface to another (such as a bed to a wheelchair). FDA UDI
Model / Reference
32475 FDA UDI
Description
The Proactive Medical patient lift is intended to transfer an individual from one resting surface to another (such as a bed to a wheelchair). FDA UDI

Identifiers

Primary DI / UDI-DI
06974512010014 FDA UDI
FDA Product Code
FSA FDA UDI
GMDN Term
Mobile patient lifting system, manual FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5510 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

No

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Mobile patient lifting system, manual

Proactive by Xiamen World Gear Sports Goods Co., Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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

Manufacturer
Xiamen World Gear Sports Goods Co., Ltd

Sources (1)

  • FDA UDI 9f1707f5-c77b-48ee-8572-1fd191ffd8d9 33 fields · synced May 30, 2026