FDA UDI In Commercial Distribution 🇺🇸 United States

Sensura Flex

DI: 05708932360012 · Model: 10103 · Coloplast A/S
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
Sensura Flex
Primary DI
05708932360012
Version / Model
10103
Catalog Number
10103
Company Name
Coloplast A/S
Labeler DUNS
305524696
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2022-12-02
Public Version
1
Public Version Date
2022-12-12
Public Version Status
New
Public Device Record Key
9ea4d3ef-961f-4d3b-a955-68b3607aebf0

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
48159 Intestinal ostomy base plate, flat

Identifiers

Type ID
Package 05708932360029
Primary 05708932360012
Unit of Use 05701780042710

Customer Contacts

Device Sizes

Type Value Unit Text
Lumen/Inner Diameter 70 Millimeter
Device Size Text, specify Base Plate Type Flat
Device Size Text, specify Coupling Size Diameter - in 2 3/4
Device Size Text, specify Base Plate Precut Start Hole Size - in 3/8
Device Size Text, specify Base Plate Precut Start Hole Size - mm 10
Device Size Text, specify Base Plate Max Cut Size - mm 68
Device Size Text, specify Base Plate Max Cut Size - in 2 11/16