FDA UDI In Commercial Distribution 🇺🇸 United States

Vortek

DI: 05701780332927 · Model: ACBM50 · Coloplast A/S
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

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Basic Information

Brand Name
Vortek
Primary DI
05701780332927
Version / Model
ACBM50
Catalog Number
ACBM50
Company Name
Coloplast A/S
Labeler DUNS
305524696
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-04-12
Public Version
1
Public Version Date
2024-04-22
Public Version Status
New
Public Device Record Key
b687e0ee-b4fa-4fde-a2aa-8654c981c8bc

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
MR Safe
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
60755 Urological surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Package 05701780332934
Primary 05701780332927
Package 05701780332958

Customer Contacts

Device Sizes

Type Value Unit Text
Catheter Gauge 4.8 French
Length 12 Centimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep away from rain. Keep away from sunlight. Do not use if package is damaged and consult IFU. Do not resterilize.