FDA UDI In Commercial Distribution 🇺🇸 United States

Self-Cath

DI: 05708932957656 · Model: 475/50785 · Coloplast A/S
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Self-Cath
Primary DI
05708932957656
Version / Model
475/50785
Catalog Number
475/50785
Company Name
Coloplast A/S
Labeler DUNS
305524696
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-02
Public Version
1
Public Version Date
2022-12-12
Public Version Status
New
Public Device Record Key
34fab807-fbd5-4b27-a325-2f9176a52723

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
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
NNX DEVICE, INCONTINENCE, UROSHEATH TYPE, NON-STERILE

GMDN Terms

Code Name
65173 Urine drainage extension tubing

Identifiers

Type ID
Package 05708932286534
Package 05708932286527
Primary 05708932957656