FDA UDI In Commercial Distribution 🇺🇸 United States

Vortek

DI: 03600040910757 · Model: ACA108 · Coloplast A/S
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Vortek
Primary DI
03600040910757
Version / Model
ACA108
Catalog Number
ACA108
Company Name
Coloplast A/S
Labeler DUNS
305524696
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-12-17
Public Version
2
Public Version Date
2022-11-07
Public Version Status
Update
Public Device Record Key
ad1c251a-46ce-438d-8271-c7859d1b878c

Device Description

Vortek . iso. Single loop ureteral stent. Ø0.035" (0.89mm). PTFE-coated guidewire / stiff.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
Yes
Not Made with NRL
No
MRI Safety
MR Conditional
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
Package 03600040910726
Package 03600040910849
Primary 03600040910757

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K201436 000