FDA UDI In Commercial Distribution 🇺🇸 United States

Coloplast

DI: 05708932702713 · Model: 14050 · Coloplast A/S
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Coloplast
Primary DI
05708932702713
Version / Model
14050
Catalog Number
14050
Company Name
Coloplast A/S
Labeler DUNS
305524696
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-03-11
Public Version
1
Public Version Date
2022-03-21
Public Version Status
New
Public Device Record Key
0c917019-4686-4db6-ad7a-258b12928b47

Device Description

Coloplast Fistula and Wound Management System / Coloplast / Coloplast Free. without filter. 1 Fistula and Wound Manager Mini. 1 Fistula Flexible Lid Mini without filter. 1 Tracing guide. 1 Transparent cover sheet. 1 Fistula Drain Port. 1 Pump per retail box. Mini. Fistula and Wound Manager Size Mini.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
MR Safe
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
FON BAG, DRAINAGE, WITH ADHESIVE, OSTOMY

GMDN Terms

Code Name
31075 One-piece intestinal ostomy bag, open-ended

Identifiers

Type ID
Package 00762123049471
Primary 05708932702713
Package 00762123049488

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Fistula and Wound Manager Size Mini

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
This way up.