Lumex

FDA UDI

Class I (US FDA UDI)

by GF Health Products, Inc

Identity

Trade Name: Lumex FDA UDI
Generic Name: Mobile patient lifting system, manual FDA UDI
Device Name: LIFT HYDRAUL HAMTONE MED SLING FDA UDI
Model / Reference: LF1031MS FDA UDI
Description: LIFT HYDRAUL HAMTONE MED SLING FDA UDI

Identifiers

Catalog Number: LF1031MS FDA UDI
Primary DI / UDI-DI: M368LF1031MS1 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Mobile patient lifting system, manual

Lumex by GF Health Products, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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BestLift — BESTCARE, L.L.C. · Class I
SARA STEDY — Arjohuntleigh, Inc. · Class I
BestMove — BESTCARE, L.L.C. · Class I
Proactive — XIAMEN WORLD GEAR SPORTS GOODS CO., LTD · Class I
Vive — VIVE HEALTH LLC · Class II
SARA STEDY — Arjohuntleigh, 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 I	Pending data

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Manufacturer

Manufacturer: GF Health Products, Inc

Sources (1)

FDA UDI 2603f641-baa8-453d-ab95-5d59dd6c2263 35 fields · synced May 30, 2026