FDA UDI Not in Commercial Distribution 🇺🇸 United States

Intersept®

DI: 00681490465939 · Model: CB1P00R · MEDTRONIC, INC.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Intersept®
Primary DI
00681490465939
Version / Model
CB1P00R
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-06-09
Public Version
4
Public Version Date
2022-12-08
Public Version Status
Update
Public Device Record Key
1c5b9ebd-f680-431a-92d8-ce69f7bc45a4
Distribution End Date
2017-11-30

Device Description

FILTER CB1P00R 2PK CB 20M W/LOOP

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
Yes
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
DTZ OXYGENATOR, CARDIOPULMONARY BYPASS

GMDN Terms

Code Name
35441 Cardiopulmonary bypass system blood tubing set

Identifiers

Type ID
Package 20681490465933
Primary 00681490465939

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K891687 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 40 Degrees Celsius