FDA UDI In Commercial Distribution 🇺🇸 United States

Coloplast

DI: 05708932730105 · Model: 00509 · Coloplast A/S
Product Codes
1
GMDN Terms
2
Identifiers
5
Pkg Device Count
10

Basic Information

Brand Name
Coloplast
Primary DI
05708932730105
Version / Model
00509
Catalog Number
00509
Company Name
Coloplast A/S
Labeler DUNS
305524696
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2022-12-07
Public Version
1
Public Version Date
2022-12-15
Public Version Status
New
Public Device Record Key
1d907ef1-c5c7-4290-bc35-ffae4927bb86

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
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
EXB COLLECTOR, OSTOMY

GMDN Terms

Code Name
31066 One-piece intestinal ostomy bag, closed-ended
31067 Multiple-piece intestinal ostomy bag, closed-ended

Identifiers

Type ID
Package 00762123042977
Package 05708932630061
Primary 05708932730105
Package 00762123042984
Unit of Use 05708932760270

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
This way up. Keep away from sunlight. Do not use if package is damaged and consult IFU.