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HealthSmart

FDA UDI

Class I (US FDA UDI)

by Dms Holdings, Inc.,

Identity

Trade Name
HealthSmart FDA UDI
Generic Name
Raised toilet seat FDA UDI
Device Name
5” Toilet Seat Riser FDA UDI
Model / Reference
522-1508-1901 FDA UDI
Description
5” Toilet Seat Riser FDA UDI

Identifiers

Primary DI / UDI-DI
00041298991496 FDA UDI
FDA Product Code
ILS FDA UDI
GMDN Term
Raised toilet seat 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Raised toilet seat

HealthSmart by Dms Holdings, Inc., — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Raised toilet seat.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dms Holdings, Inc.,

Sources (1)

  • FDA UDI 0e14ae62-7262-43ed-89b0-cfc018a0f274 33 fields · synced May 30, 2026