FDA UDI In Commercial Distribution 🇺🇸 United States

Venovo®

DI: 00801741103667 · Model: VENUL16120 · Angiomed GmbH & Co. Medizintechnik KG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Venovo®
Primary DI
00801741103667
Version / Model
VENUL16120
Catalog Number
VENUL16120
Company Name
Angiomed GmbH & Co. Medizintechnik KG
Labeler DUNS
320047483
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-18
Public Version
2
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
7ec9e247-4a36-4e30-998e-f5b6ef8b84dc

Device Description

Venovo® Venous Stent System 16 mm x 120 mm (120 cm delivery catheter)

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
QAN Stent, iliac vein

GMDN Terms

Code Name
58057 Iliofemoral vein stent

Identifiers

Type ID
Primary 00801741103667

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Implant Length, 120 Millimeter
Device Size Text, specify Implant Diameter, 16 Millimeter
Device Size Text, specify Catheter Length, 120 Centimeter