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Invisia™ SerenaSeat™ Pro

FDA UDI

Class I (US FDA UDI)

by Healthcraft Products Inc.

Identity

Trade Name
Invisia™ SerenaSeat™ Pro FDA UDI
Generic Name
Shower seat, non-powered FDA UDI
Device Name
The Serena-Seat is a high quality, commercial grade, fold down shower seat. The Serena-Seat is intended to provide shower seating support for people with reduced mobility. The Serena-Seat is intended to bear weight ONLY when the seat is in the down position; the seat is not intended to bear weight in any other position. The Serena-Seat is intended to be folded up when not in use. A friction hinge ensures that the seat will not inadvertently lower when it is in the up position. To adjust the amount of friction required to fold seat, remove end cap and turn finger nut. The Serena-Seat is installed with appropriate fasteners to a structural wall. The maximum user weight for this product is 500lbs / 227kgs. Note: Product is not intended to support full body weight (i.e. do not stand on the seat). FDA UDI
Model / Reference
INV-WSFD-26-MEDIUM-ORB FDA UDI
Description
The Serena-Seat is a high quality, commercial grade, fold down shower seat. The Serena-Seat is intended to provide shower seating support for people with reduced mobility. The Serena-Seat is intended to bear weight ONLY when the seat is in the down position; the seat is not intended to bear weight in any other position. The Serena-Seat is intended to be folded up when not in use. A friction hinge ensures that the seat will not inadvertently lower when it is in the up position. To adjust the amount of friction required to fold seat, remove end cap and turn finger nut. The Serena-Seat is installed with appropriate fasteners to a structural wall. The maximum user weight for this product is 500lbs / 227kgs. Note: Product is not intended to support full body weight (i.e. do not stand on the seat). FDA UDI

Identifiers

Primary DI / UDI-DI
00689281035347 FDA UDI
FDA Product Code
IKX FDA UDI
GMDN Term
Shower seat, non-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5050 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Shower seat, non-powered

Invisia™ SerenaSeat™ Pro by Healthcraft Products Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Shower seat, non-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d0a83c61-2a4c-4da7-94c5-e17535350845 33 fields · synced May 29, 2026