FDA UDI In Commercial Distribution 🇺🇸 United States

SenSura Mio

DI: 05701780253758 · Model: 18390 · Coloplast A/S
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
SenSura Mio
Primary DI
05701780253758
Version / Model
18390
Catalog Number
18390
Company Name
Coloplast A/S
Labeler DUNS
305524696
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2022-02-18
Public Version
2
Public Version Date
2022-12-07
Public Version Status
Update
Public Device Record Key
7fa37ccb-549b-427f-868d-8eeb243081da

Device Description

SenSura Mio . 2-piece.

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 05701780255103
Primary 05701780253758
Unit of Use 05701780255875

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Base Plate Precut Start Hole Size - mm 10
Lumen/Inner Diameter 90 Millimeter
Device Size Text, specify Base Plate Type Flat
Device Size Text, specify Base Plate Precut Start Hole Size - in 3/8
Device Size Text, specify Coupling Size Diameter - in 3 9/16