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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 36-inch wide mattress FDA UDI
Model / Reference
EAS-36-Z FDA UDI
Description
EasyShift Repositioning System V3 for 36-inch wide mattress FDA UDI

Identifiers

Primary DI / UDI-DI
00860004936848 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, hydraulicAlternating-pressure bed mattress system remote control

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

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Manufacturer

Manufacturer
Seneca Devices Inc

Sources (1)

  • FDA UDI 01a96e54-d102-4b1b-ae3a-ee3b4f3648a0 33 fields · synced May 29, 2026