FDA UDI In Commercial Distribution 🇺🇸 United States

SenSura Mio

DI: 05701780357722 · Model: 19733 · Coloplast A/S
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
30

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
SenSura Mio
Primary DI
05701780357722
Version / Model
19733
Catalog Number
19733
Company Name
Coloplast A/S
Labeler DUNS
305524696
Distribution Status
In Commercial Distribution
Device Count in Pkg
30
Record Status
Published
Publish Date
2025-11-20
Public Version
1
Public Version Date
2025-11-28
Public Version Status
New
Public Device Record Key
f0ae0e95-67b8-4bab-a111-febc0579ad56

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
31067 Multiple-piece intestinal ostomy bag, closed-ended

Identifiers

Type ID
Package 05701780357739
Primary 05701780357722
Unit of Use 05701780357746

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Coupling Size Diameter - in 2 3/4
Lumen/Inner Diameter 70 Millimeter
Device Size Text, specify Descriptive Bag Size Maxi

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep away from sunlight.