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GoodSense

FDA UDI

Class I (US FDA UDI)

by Geiss, Destin & Dunn, Inc

Identity

Trade Name
GoodSense FDA UDI
Generic Name
Non-woven gauze pad FDA UDI
Device Name
Sterile Pads, all one size, 3 IN x 3 IN (76 mm x 76 mm) FDA UDI
Model / Reference
180410000880 FDA UDI
Description
Sterile Pads, all one size, 3 IN x 3 IN (76 mm x 76 mm) FDA UDI

Identifiers

Primary DI / UDI-DI
00180410000880 FDA UDI
FDA Product Code
NAB FDA UDI
GMDN Term
Non-woven gauze pad FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4014 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Category: Non-woven gauze pad

GoodSense by Geiss, Destin & Dunn, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-woven gauze pad.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ff225e37-8fe7-4e4d-b6bf-b70a08bd1a03 34 fields · synced May 30, 2026