FDA Registration Active 🇺🇸 United States

Medtronic2686 (MN) - Visi-Pro Ballon-expandable Peripheral Stent System

Reg #: 2183744 · FEI: 2183744 · Expires 2025
Products
1
Proprietary Names
1
Establishment Types
1
Classifications
1

Registration Details

Registration Name
Isomedix Operations, Inc.
Registration Number
2183744
FEI Number
2183744
Status
Active
Expiry Year
2025
Initial Importer
No
Address
380 90TH AVE NW
City
Minneapolis
State
MN
ZIP
55433
Country
US

Regulatory Submissions

PMA Number
P030045

Owner / Operator

Firm Name
STERIS Corporation
Operator Number
1527821
Address
5960 Heisley Rd, --
City
Mentor
State
OH
Postal Code
44060
Country
US

Products

Device Name Product Code
Stent, Iliac NIO

Proprietary Names

Medtronic2686 (MN) - Visi-Pro Ballon-expandable Peripheral Stent System

Establishment Types

Sterilize Medical Device for Another Party (Contract Sterilizer)