FDA UDI In Commercial Distribution 🇺🇸 United States

Porges Coloplast

DI: 03600040201534 · Model: AJ4973 · Coloplast A/S
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Porges Coloplast
Primary DI
03600040201534
Version / Model
AJ4973
Catalog Number
AJ4973
Company Name
Coloplast A/S
Labeler DUNS
305524696
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
4
Public Version Date
2023-04-03
Public Version Status
Update
Public Device Record Key
bccd3abd-5a52-4dd5-8218-afcc9cb17f5e

Device Description

Double loop ureteral stent in silicone open/closed CH FR 07 length 24 cm with non connectable pusher and fixed core guidewire

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FAD STENT, URETERAL

GMDN Terms

Code Name
58005 Polymeric ureteral stent

Identifiers

Type ID
Primary 03600040201534

Customer Contacts

Device Sizes

Type Value Unit Text
Catheter Gauge 7 French
Length 24 Centimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store away from light in a cool and dry place