FDA UDI In Commercial Distribution 🇺🇸 United States

MC2®

DI: 00643169463035 · Model: 91329 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
MC2®
Primary DI
00643169463035
Version / Model
91329
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-16
Public Version
4
Public Version Date
2022-08-05
Public Version Status
Update
Public Device Record Key
57c571d7-0c10-43a6-98eb-6924884be34a

Device Description

CANNULA 91329 MC2 VEN 29/29FR 10PK 17L

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
34905 Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, venous

Identifiers

Type ID
Package 20643169463039
Primary 00643169463035

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K140165 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 29-29 FR