Handi-Move Slide

FDA UDI

Class I (US FDA UDI)

by Handi-Move

Identity

Trade Name: Handi-Move Slide FDA UDI
Generic Name: Manual patient lifting belt/harness FDA UDI
Device Name: Handi handling belt 3608 FDA UDI
Model / Reference: 3608 00000001 FDA UDI
Description: Handi handling belt 3608 FDA UDI

Identifiers

Catalog Number: 3608 00000001 FDA UDI
Primary DI / UDI-DI: 05404016612601 FDA UDI
FDA Product Code: FMR FDA UDI
GMDN Term: Manual patient lifting belt/harness FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.6785 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Manual patient lifting belt/harness

Handi-Move Slide by Handi-Move — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual patient lifting belt/harness.

Binder Lift — We Stitch Stuff, LLC · Class I
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AirWedge — Hovertech International · Class II
Mobi-tools Grip — MEDI CARE SYSTEM SLU · Class I
Binder Lift — We Stitch Stuff, LLC · Class I
Mobi-tools Grip — MEDI CARE SYSTEM SLU · Class I
Binder Lift — We Stitch Stuff, LLC · Class I
Binder Lift — We Stitch Stuff, LLC · 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: Handi-Move

Sources (1)

FDA UDI 30cce43b-4fa0-4bcc-9b2e-7327604b040d 35 fields · synced Jun 1, 2026