FDA UDI In Commercial Distribution 🇺🇸 United States

EverFlex

DI: 00821684033760 · Model: PRB35-06-030-080 · Covidien LP
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EverFlex
Primary DI
00821684033760
Version / Model
PRB35-06-030-080
Company Name
Covidien LP
Labeler DUNS
968903703
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-22
Public Version
7
Public Version Date
2023-02-03
Public Version Status
Update
Public Device Record Key
b6d00c23-d695-4e7b-824c-b772d403fcd1

Device Description

Self-Expanding Peripheral Stent System

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
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NIP STENT, SUPERFICIAL FEMORAL ARTERY

GMDN Terms

Code Name
47932 Peripheral artery stent, bare-metal

Identifiers

Type ID
Primary 00821684033760

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P110023 004

Device Sizes

Type Value Unit Text
Length 30 Millimeter
Catheter Gauge 6 French
Device Size Text, specify Working Length,80,Centimeter;Compatible Guidewire,.035,Inch;Lumen Diameter,4.5 to 5.5,Millimeter;
Outer Diameter 6 Millimeter
Outer Diameter 2 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry