PremierPro

FDA UDI

Class I (US FDA UDI)

by Svs Llc

Identity

Trade Name: PremierPro FDA UDI
Generic Name: Patient transfer system, manual FDA UDI
Device Name: PremierPro Tubular Slide Sheets 1/bag FDA UDI
Model / Reference: 3790 FDA UDI
Description: PremierPro Tubular Slide Sheets 1/bag FDA UDI

Identifiers

Catalog Number: 3790 FDA UDI
Primary DI / UDI-DI: 00811220033453 FDA UDI
FDA Product Code: FMR FDA UDI
GMDN Term: Patient transfer system, manual 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

Yes

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

Yes

FDA UDI

Category: Patient transfer system, manual

PremierPro by Svs 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: Svs Llc

Sources (1)

FDA UDI 3bbb8759-4b33-4dee-a50b-eda1ff6d9914 35 fields · synced May 31, 2026