FDA UDI In Commercial Distribution 🇺🇸 United States

CLEARVIEW®

DI: 20885074257451 · Model: 31250 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
CLEARVIEW®
Primary DI
20885074257451
Version / Model
31250
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2020-07-27
Public Version
2
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
9c6063d8-71c5-493b-a4d0-a8f30393babc

Device Description

SHUNT 31250 ARTERIOTOMY 2.50MM 5PK 15LA

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
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
DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass

GMDN Terms

Code Name
13586 Arteriovenous shunt

Identifiers

Type ID
Unit of Use 00885074257457
Primary 20885074257451

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K120612 000

Device Sizes

Type Value Unit Text
Outer Diameter 2.5 Millimeter