FDA UDI In Commercial Distribution 🇺🇸 United States

Assura

DI: 05708932131124 · Model: 13620 · Coloplast A/S
Product Codes
1
GMDN Terms
2
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Assura
Primary DI
05708932131124
Version / Model
13620
Catalog Number
13620
Company Name
Coloplast A/S
Labeler DUNS
305524696
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-05
Public Version
1
Public Version Date
2022-12-13
Public Version Status
New
Public Device Record Key
167f32c0-db8a-4082-b300-c64f52cd3223

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
Yes
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EXB COLLECTOR, OSTOMY

GMDN Terms

Code Name
48158 Intestinal ostomy base plate, convex
31076 Multiple-piece intestinal ostomy bag, open-ended

Identifiers

Type ID
Package 05708932131315
Primary 05708932131124

Customer Contacts

Device Sizes

Type Value Unit Text
Total Volume 655 Milliliter
Device Size Text, specify Base Plate Type Convex Light
Device Size Text, specify Coupling Size Diameter - in 2 3/8
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 43
Device Size Text, specify Base Plate Max Cut Size - in 1 11/16
Lumen/Inner Diameter 60 Millimeter