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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
Disposable Transfer Mat, REMUV, 36" FDA UDI
Model / Reference
3770 FDA UDI
Description
Disposable Transfer Mat, REMUV, 36" FDA UDI

Identifiers

Catalog Number
3770 FDA UDI
Primary DI / UDI-DI
00811220032357 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

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 36 Inch FDA UDI

Category: Patient transfer system, manual

PremierPro by Svs Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient transfer system, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Svs Llc

Sources (1)

  • FDA UDI 9afaeb7e-1225-42b7-af41-c29e17cd5712 37 fields · synced May 31, 2026