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EasyShift Sheet

FDA UDI

Class I (US FDA UDI)

by Seneca Devices Inc

Identity

Trade Name
EasyShift Sheet FDA UDI
Generic Name
Patient transfer/turning sheet, single-use FDA UDI
Device Name
EasyShift SPU Zipper Sheet FDA UDI
Model / Reference
EAS-Z-SPU FDA UDI
Description
EasyShift SPU Zipper Sheet FDA UDI

Identifiers

Primary DI / UDI-DI
00860004936862 FDA UDI
FDA Product Code
FMR FDA UDI
GMDN Term
Patient transfer/turning sheet, single-use 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Patient transfer/turning sheet, single-use

EasyShift Sheet by Seneca Devices Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient transfer/turning sheet, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Seneca Devices Inc

Sources (1)

  • FDA UDI 21d25417-1383-484e-a48c-35bbde014436 33 fields · synced May 31, 2026