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Jay GO Back

FDA UDI

Class I (US FDA UDI)

by Sunrise Medical (US) LLC

Identity

Trade Name
Jay GO Back FDA UDI
Generic Name
Wheelchair seat cushion FDA UDI
Device Name
The JAY GO wheelchair back features an easy to install Velcro® strap assembly, Dartex® moisture-resistant cover and wide straps for tension-adjustable support. FDA UDI
Model / Reference
Jay GO FDA UDI
Description
The JAY GO wheelchair back features an easy to install Velcro® strap assembly, Dartex® moisture-resistant cover and wide straps for tension-adjustable support. FDA UDI

Identifiers

Catalog Number
E2611, E2612 FDA UDI
Primary DI / UDI-DI
00016958053555 FDA UDI
FDA Product Code
IMP FDA UDI
GMDN Term
Wheelchair seat cushion FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3920 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Wheelchair seat cushion

Jay GO Back by Sunrise Medical (US) LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wheelchair seat cushion.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 42097c01-8a02-4cb0-ba93-dd34b4e0964d 34 fields · synced Jun 9, 2026