Patient Shifter: Kit Aqua W/ Hanger And Pull Strap

FDA UDI

Class I (US FDA UDI)

by AliMed, LLC

Identity

Trade Name: PATIENT SHIFTER: KIT AQUA W/ HANGER AND PULL STRAP FDA UDI
Generic Name: Patient transfer sliding board FDA UDI
Model / Reference: 924895 FDA UDI

Identifiers

Catalog Number: 2970012391 FDA UDI
Primary DI / UDI-DI: 00733657282948 FDA UDI
FDA Product Code: IKX FDA UDI
GMDN Term: Patient transfer sliding board 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Patient transfer sliding board

Patient Shifter: Kit Aqua W/ Hanger And Pull Strap by AliMed, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: AliMed, LLC

Sources (1)

FDA UDI 45eb7844-82f8-43c5-8c3f-a944f4cf681b 34 fields · synced Jun 9, 2026