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JayFit Back

FDA UDI

Class I (US FDA UDI)

by Sunrise Medical (US) LLC

Identity

Trade Name
JayFit Back FDA UDI
Generic Name
Gel-filled chair cushion FDA UDI
Device Name
JAY® Fit Seating simplifies the world of made-to-order seating by offering a "semi-personalized" solution. A great option for individuals who require more complex seating than off-the-shelf options can provide that still allows for adjustments and growth. FDA UDI
Model / Reference
Fit Back FDA UDI
Description
JAY® Fit Seating simplifies the world of made-to-order seating by offering a "semi-personalized" solution. A great option for individuals who require more complex seating than off-the-shelf options can provide that still allows for adjustments and growth. FDA UDI

Identifiers

Catalog Number
Jay FDA UDI
Primary DI / UDI-DI
00016958042580 FDA UDI
FDA Product Code
IMP FDA UDI
GMDN Term
Gel-filled chair cushion FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3920 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 57ccb53b-1778-4284-ab29-3ddea493aac1 35 fields · synced Jun 9, 2026