FDA UDI In Commercial Distribution 🇺🇸 United States

Intersept®

DI: 40613994352871 · Model: 6030 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
20

Basic Information

Brand Name
Intersept®
Primary DI
40613994352871
Version / Model
6030
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2016-06-17
Public Version
4
Public Version Date
2022-12-08
Public Version Status
Update
Public Device Record Key
3de30a5e-79a2-4ee6-93dd-79b369aa8565

Device Description

CONN 6030 1/4X1/4X1/4 Y 20CT 8L

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
DWE TUBING, PUMP, CARDIOPULMONARY BYPASS

GMDN Terms

Code Name
35441 Cardiopulmonary bypass system blood tubing set

Identifiers

Type ID
Primary 40613994352871
Unit of Use 00613994352873

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K800178 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 6.4 MM Port Outer Diameter