FDA UDI Not in Commercial Distribution 🇺🇸 United States

VC2™

DI: 20643169081677 · Model: 93451 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
VC2™
Primary DI
20643169081677
Version / Model
93451
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2016-06-17
Public Version
4
Public Version Date
2022-08-05
Public Version Status
Update
Public Device Record Key
0f20997b-804c-479f-8d63-9609f6f42dc6
Distribution End Date
2017-08-25

Device Description

CANNULA 93451 VC2 VEN 34/51FR 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
Primary 20643169081677
Unit of Use 00643169081673

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K845045 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 34-51 FR