FDA UDI Not in Commercial Distribution 🇺🇸 United States

Intersept®

DI: 00613994529084 · Model: CB1351 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Intersept®
Primary DI
00613994529084
Version / Model
CB1351
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
2020-01-22
Public Version Status
Update
Public Device Record Key
96d6929e-f85d-44b0-802a-d6ed793e4f86
Distribution End Date
2016-09-14

Device Description

RESERVOIR CB1351 BIOACT CARDIOTOM US 6PK

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
DTZ OXYGENATOR, CARDIOPULMONARY BYPASS

GMDN Terms

Code Name
31710 Cardiotomy reservoir

Identifiers

Type ID
Package 20613994529088
Primary 00613994529084

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K926226 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 40 Degrees Celsius