Superslide

FDA UDI

Class I (US FDA UDI)

by Therafin Corporation

Identity

Trade Name: Superslide FDA UDI
Generic Name: Patient transfer sliding board FDA UDI
Device Name: TRANSFER BOARD, SUPERSLIDE, 24 FDA UDI
Model / Reference: 31604 FDA UDI
Description: TRANSFER BOARD, SUPERSLIDE, 24 FDA UDI

Identifiers

Catalog Number: 31604 FDA UDI
Primary DI / UDI-DI: 00840252910166 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

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

Superslide by Therafin Corporation — 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: Therafin Corporation

Sources (1)

FDA UDI 9383ea2b-8b15-4804-80e6-48b756b8d4eb 35 fields · synced May 30, 2026