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E-Z Scrub

FDA UDI

Class I (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
E-Z Scrub FDA UDI
Generic Name
Surgical scrub brush, single-use FDA UDI
Device Name
E-Z Scrub 160 Surgical Scrub Brush/Sponge with Nail Cleaner - No Detergent FDA UDI
Model / Reference
371603 FDA UDI
Description
E-Z Scrub 160 Surgical Scrub Brush/Sponge with Nail Cleaner - No Detergent FDA UDI

Identifiers

Catalog Number
371603 FDA UDI
Primary DI / UDI-DI
00382903716036 FDA UDI
FDA Product Code
GEC FDA UDI
GMDN Term
Surgical scrub brush, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical scrub brush, single-use

E-Z Scrub by Becton Dickinson And Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical scrub brush, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 97022706-9627-4a2e-adca-6d133ac518d6 36 fields · synced May 30, 2026