← Back to catalogue

Shower Seat

FDA UDI

Class I (US FDA UDI)

by Ropox A/S

Identity

Trade Name
Shower Seat FDA UDI
Generic Name
Shower seat, non-powered FDA UDI
Model / Reference
Backrest, with Arm Support FDA UDI

Identifiers

Catalog Number
40-43025-3 FDA UDI
Primary DI / UDI-DI
05707581000775 FDA UDI
FDA Product Code
INN FDA UDI
GMDN Term
Shower seat, non-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3100 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

Yes

FDA UDI

Category: Shower seat, non-powered

Shower Seat by Ropox A/S — 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

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

Manufacturer

Manufacturer
Ropox A/S

Sources (1)

  • FDA UDI d0ebcfe0-4707-4380-b685-9fc064b356f1 34 fields · synced Jun 1, 2026