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Dalton Toilet Seat

FDA UDI

Class I (US FDA UDI)

by Dalton Medical Corp.

Identity

Trade Name
DALTON TOILET SEAT FDA UDI
Generic Name
Raised toilet seat FDA UDI
Device Name
RAISED TOILET SEAT FDA UDI
Model / Reference
BS-30271G-1 FDA UDI
Description
RAISED TOILET SEAT FDA UDI

Identifiers

Primary DI / UDI-DI
00815027012840 FDA UDI
FDA Product Code
INB FDA UDI
GMDN Term
Raised toilet seat FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3920 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

No

FDA UDI

Category: Raised toilet seat

Dalton Toilet Seat by Dalton Medical Corp. — 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

Sources (1)

  • FDA UDI b5a3bd91-3370-40bc-9fc2-237349911739 33 fields · synced May 30, 2026