Brava

Primary DI
05708932513661
Brand
Brava
Company
Coloplast A/S
Model
120610
Catalog number
120610
Device description
Brava Lubricating Deodorant / Brava / Brava Protective Sheet / Brava Odor neutralizer. Multi-lubricating effect. 1. Shake the bottle well before use. 2. Add 5-10 ml in the bag and rub the bag gently to spread Brava Lubricating Deodorant evenly. If you use an open bag you can also add the deodorant through the outlet. 3. Repeat after emptying the bag.. Mandatory text BR 1. Ostomy Care. Volume 240 ml.
Published
2021-05-14
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
true
Sterile
false
Single use
false

Contact Domains#

Product Codes#

Code, Name table
CodeName
NECBandage, liquid, skin protectant

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
NECBandage, Liquid, Skin ProtectantGeneral Hospital1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
05708932513661PackageGS116In Commercial Distribution
05708932513654PrimaryGS10
05708932750189PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
05708932513661057089325136615708932513661
05708932513654057089325136545708932513654
05708932750189057089327501895708932750189

GMDN Terms#

Term, Definition table
TermDefinition
Ostomy odour-absorbent/deodorizerA device used by an ostomate to absorb unwanted odours and/or emit fragrance to conceal any unpleasant odours emanating from their stoma/ostomy devices. It is available in various forms, such as a powder with anti-odour properties (e.g., Zeolite) or a portable spray, for convenient daily use. After application this device cannot be reused.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Total Volume240Milliliter

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+1(800)533-0464healthcarecs@coloplast.com

Regulatory Flags#

DUNS number
305524696
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
false
Sterilization required before use
false

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