← Back to catalogue

EasyShift

FDA UDI

Class I (US FDA UDI)

by Seneca Devices Inc

Identity

Trade Name
EasyShift FDA UDI
Generic Name
Bed mattress support platform, hydraulic FDA UDI
Device Name
EasyShift Repositioning System V3 for 42" wide mattress, compatible with EasyShift Zipper Sheet FDA UDI
Model / Reference
EAS-42-Z FDA UDI
Description
EasyShift Repositioning System V3 for 42" wide mattress, compatible with EasyShift Zipper Sheet FDA UDI

Identifiers

Primary DI / UDI-DI
00860004936817 FDA UDI
FDA Product Code
FNK FDA UDI
IKZ FDA UDI
GMDN Term
Bed mattress support platform, hydraulic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5110 FDA UDI
890.5225 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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: Bed mattress support platform, hydraulicIntensive-care patient transport system, ventilatory support, neonatal

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

Similar devices

Also classified as Bed mattress support platform, hydraulic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Seneca Devices Inc

Sources (1)

  • FDA UDI b18f338a-997e-4b97-9335-674754af5dee 33 fields · synced Jun 6, 2026