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Tincture of Benzoin Spray 4oz US

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew Medical, Ltd.

Identity

Trade Name
Tincture of Benzoin Spray 4oz US FDA UDI
Generic Name
Patient medical adhesive remover FDA UDI
Device Name
Tincture of Benzoin Skin Prep Spray is a skin prep spray that enhances the adhesion of tape/appliance while protecting sensitive skin from adhesives and body fluids. FDA UDI
Model / Reference
407000 FDA UDI
Description
Tincture of Benzoin Skin Prep Spray is a skin prep spray that enhances the adhesion of tape/appliance while protecting sensitive skin from adhesives and body fluids. FDA UDI

Identifiers

Catalog Number
407000 FDA UDI
Primary DI / UDI-DI
00040565111827 FDA UDI
FDA Product Code
FON FDA UDI
GMDN Term
Patient medical adhesive remover FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.5900 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Patient medical adhesive remover

Tincture of Benzoin Spray 4oz US by Smith & Nephew Medical, Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient medical adhesive remover.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cfcf0166-06bc-4c87-90ca-d324fd199e3c 34 fields · synced May 30, 2026