FDA UDI In Commercial Distribution 🇺🇸 United States

Coloplast

DI: 00762123032282 · Model: 21365 · Coloplast A/S
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
Coloplast
Primary DI
00762123032282
Version / Model
21365
Catalog Number
21365
Company Name
Coloplast A/S
Labeler DUNS
305524696
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2022-12-05
Public Version
1
Public Version Date
2022-12-13
Public Version Status
New
Public Device Record Key
4a4415eb-ebdf-493a-872d-01bd3f01c96a

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NNW BAG, URINE COLLECTION, LEG, FOR EXTERNAL USE, NON-STERILE

GMDN Terms

Code Name
58921 Non-wearable adult urine collection bag, open-ended

Identifiers

Type ID
Package 00762123032299
Primary 00762123032282
Unit of Use 05701780055567

Customer Contacts

Device Sizes

Type Value Unit Text
Total Volume 2000 Milliliter
Length 120 Centimeter