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GoodSense

FDA UDI

Class U (US FDA UDI)

by Geiss, Destin & Dunn, Inc

Identity

Trade Name
GoodSense FDA UDI
Generic Name
Wound irrigation sterile saline FDA UDI
Device Name
Sterile Saline Wound Wash. Packaged in an Aerosol (BOV) can. FDA UDI
Model / Reference
2720 FDA UDI
Description
Sterile Saline Wound Wash. Packaged in an Aerosol (BOV) can. FDA UDI

Identifiers

Primary DI / UDI-DI
00846036002720 FDA UDI
FDA Product Code
FRO FDA UDI
FQH FDA UDI
GMDN Term
Wound irrigation sterile saline FDA UDI

Classification

Device Class
U FDA UDI
Regulation Number
880.5475 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Wound irrigation sterile saline

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

Similar devices

Also classified as Wound irrigation sterile saline.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 615e2ae8-8bc2-4fb7-a26d-e925afd115d4 35 fields · synced Jun 8, 2026