FDA UDI In Commercial Distribution 🇺🇸 United States

Coloplast

DI: 00762123049570 · Model: 14031 · Coloplast A/S
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
Coloplast
Primary DI
00762123049570
Version / Model
14031
Catalog Number
14031
Company Name
Coloplast A/S
Labeler DUNS
305524696
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2022-03-11
Public Version
2
Public Version Date
2023-03-13
Public Version Status
Update
Public Device Record Key
c52bf352-80a4-4d78-a967-dfaea9d9ea86

Device Description

Coloplast Flexible lid / Coloplast / Coloplast Fistula Flexible Lid. without filter. The manufacturer recommends the sole use. Midi. Fistula and Wound Manager Size Midi.

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 00762123049587
Primary 00762123049570
Unit of Use 05708932761772

Customer Contacts

Device Sizes

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