FDA.reportPublic FDA data

E-Z Scrub

Primary DI
50382903716031
Brand
E-Z Scrub
Company
BECTON, DICKINSON AND COMPANY
Model
371603
Catalog number
371603
Device description
E-Z Scrub 160 Surgical Scrub Brush/Sponge with Nail Cleaner - No Detergent
Published
2020-02-04
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
false
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
GECBRUSH, SCRUB, OPERATING-ROOM

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
GECBrush, Scrub, Operating-RoomGeneral, Plastic Surgery1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
30382903716037PackageGS130In Commercial Distribution
50382903716031PackageGS110In Commercial Distribution
00382903716036PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
3038290371603730382903716037
5038290371603150382903716031
00382903716036003829037160363829037160360382903716036

GMDN Terms#

Term, Definition table
TermDefinition
Surgical scrub brush, single-useA hand-held device used by hospital staff to scrub their hands, fingers, and forearms prior to surgery or other intervention where a high degree of personal hygiene is required; it may also be used to mechanically clean the intact skin or superficial wounds of a patient. This device typically has a synthetic sponge surface and a soft bristle surface; it may also include a separate nail cleaner and/or a disinfecting substance. This is a single-use device.

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Special Storage Condition, Specify00Avoid excessive heat 40°C (104°F)

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+1(800)523-0502Customer_Support@BD.com
+1(800)453-4538Customer_Support@BD.com

Regulatory Flags#

DUNS number
124987988
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
true
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00382906718167Horizon6718166718162026-09-24
00382906718174Horizon6718176718172026-09-24
00382906718181Horizon6718186718182026-09-24
00382906718198Horizon6718196718192026-09-24
00382906718204Horizon6718206718202026-09-24
00382906718211Horizon6718216718212026-09-24
00382906718235Horizon6718236718232026-09-24
00382906718242Horizon6718246718242026-09-24
00382906718259Horizon6718256718252026-09-24
00382906718266Horizon6718266718262026-09-24
00382906718273Horizon6718276718272026-09-24
00382906718280Horizon6718286718282026-09-24
00382906718310Horizon6718316718312026-09-24
00382906718327Horizon6718326718322026-09-24
00382906718334Horizon6718336718332026-09-24
00382906718341Horizon6718346718342026-09-24
00382906718358Not Applicable6718356718352026-09-24
00382906718365Horizon6718366718362026-09-24
00382906718372Horizon6718376718372026-09-24
00382906718389Horizon6718386718382026-09-24

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Primary DI, Brand, Company table
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