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Plus

FDA UDI

Class I (US FDA UDI)

by Pressalit A/S

Identity

Trade Name
PLUS FDA UDI
Generic Name
Shower seat, non-powered FDA UDI
Device Name
PLUS shower seat 450, with aperture, incl. backrest, lime green. Manually height and sideways adjustable, for fitting to horizontal wall track FDA UDI
Model / Reference
R7455 FDA UDI
Description
PLUS shower seat 450, with aperture, incl. backrest, lime green. Manually height and sideways adjustable, for fitting to horizontal wall track FDA UDI

Identifiers

Catalog Number
R7455277 FDA UDI
Primary DI / UDI-DI
05708590359991 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

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: Shower seat, non-powered

Plus by Pressalit 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

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Manufacturer

Manufacturer
Pressalit A/S

Sources (1)

  • FDA UDI 053440a6-9e0a-4e0c-91b1-b704635810b9 35 fields · synced May 30, 2026