FDA UDI In Commercial Distribution 🇺🇸 United States

MC2™

DI: 00643169696938 · Model: CB91265C · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MC2™
Primary DI
00643169696938
Version / Model
CB91265C
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-03-04
Public Version
4
Public Version Date
2022-08-05
Public Version Status
Update
Public Device Record Key
0218e96c-5a0f-4aad-b354-857c936792d2

Device Description

CANN CB91265C MC2 36/46FR CON

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
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

GMDN Terms

Code Name
34905 Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, venous

Identifiers

Type ID
Primary 00643169696938

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K140165 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 36-46 FR

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 40 Degrees Celsius