FDA UDI In Commercial Distribution 🇺🇸 United States

SenSura Mio

DI: 05701780358026 · Model: 19758 · Coloplast A/S
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

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
05701780358026
Version / Model
19758
Catalog Number
19758
Company Name
Coloplast A/S
Labeler DUNS
305524696
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
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
a91a790f-b864-4081-a094-bf784bd57f10

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
31076 Multiple-piece intestinal ostomy bag, open-ended

Identifiers

Type ID
Package 05701780358033
Primary 05701780358026
Unit of Use 05701780358040

Customer Contacts

Device Sizes

Type Value Unit Text
Lumen/Inner Diameter 40 Millimeter
Device Size Text, specify Descriptive Bag Size Midi
Device Size Text, specify Coupling Size Diameter - in 1 5/8

Storage Conditions

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