GoodSense

FDA UDI

Class I (US FDA UDI)

by Geiss, Destin & Dunn, Inc

Identity

Trade Name: GoodSense FDA UDI
Generic Name: Pressure bandage, non-latex, single-use FDA UDI
Device Name: Tender Tape, 2 IN x 5 YDS (50 mm x 4.5 m) stretched; 2 IN x 2.2 YDS (50 mm x 2 m) FDA UDI
Model / Reference: 180410000231 FDA UDI
Description: Tender Tape, 2 IN x 5 YDS (50 mm x 4.5 m) stretched; 2 IN x 2.2 YDS (50 mm x 2 m) FDA UDI

Identifiers

Primary DI / UDI-DI: 00180410000231 FDA UDI
FDA Product Code: FQM FDA UDI
GMDN Term: Pressure bandage, non-latex, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.5075 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Pressure bandage, non-latex, single-use

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Geiss, Destin & Dunn, Inc

Sources (1)

FDA UDI 39c4a3d8-4076-4dec-9069-7704925c5f67 33 fields · synced May 30, 2026