← Back to catalogue

Dalton Underpad

FDA UDI

Class I (US FDA UDI)

by Dalton Medical Corp.

Identity

Trade Name
DALTON UNDERPAD FDA UDI
Generic Name
Absorbent underpad, non-antimicrobial, single-use FDA UDI
Device Name
UNDERPAD 30X36, 100/CS, PINK 94G FDA UDI
Model / Reference
IN-AUP12090 FDA UDI
Description
UNDERPAD 30X36, 100/CS, PINK 94G FDA UDI

Identifiers

Primary DI / UDI-DI
00815027012611 FDA UDI
FDA Product Code
HHD FDA UDI
GMDN Term
Absorbent underpad, non-antimicrobial, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.5435 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Absorbent underpad, non-antimicrobial, single-use

Dalton Underpad by Dalton Medical Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Absorbent underpad, non-antimicrobial, single-use.

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

Sources (1)

  • FDA UDI 47aedf88-f4f9-4d59-8fb5-b6213c6fc558 33 fields · synced May 31, 2026