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Bathtub

FDA UDI

Class I (US FDA UDI)

by Ropox A/S

Identity

Trade Name
Bathtub FDA UDI
Generic Name
Height-adjustable bathtub FDA UDI
Model / Reference
Electric, 180x80cm FDA UDI

Identifiers

Catalog Number
40-14158-2 FDA UDI
Primary DI / UDI-DI
05707581000393 FDA UDI
FDA Product Code
IKX FDA UDI
GMDN Term
Height-adjustable bathtub 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Height-adjustable bathtub

Bathtub by Ropox A/S — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Height-adjustable bathtub.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ropox A/S

Sources (1)

  • FDA UDI 7585dbd4-d9bf-4e12-9fb4-242de976d870 34 fields · synced Jun 8, 2026