FDA UDI In Commercial Distribution 🇺🇸 United States

ClearView™

DI: 00763000631437 · Model: 31200 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ClearView™
Primary DI
00763000631437
Version / Model
31200
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-04-12
Public Version
1
Public Version Date
2026-04-20
Public Version Status
New
Public Device Record Key
e7f82a8d-f21d-44a8-8088-4e867b0ae258

Device Description

SHUNT 31200 ARTERIOTOMY 2.00MM 5PK

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
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
DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass

GMDN Terms

Code Name
47111 Surgical intravascular shunt

Identifiers

Type ID
Package 20763000631431
Primary 00763000631437

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K253998 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Tip diameters: 2.00 mm