FDA UDI Not in Commercial Distribution 🇺🇸 United States

DLP®

DI: 00673978864921 · Model: CB96021 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DLP®
Primary DI
00673978864921
Version / Model
CB96021
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-29
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
2da08537-36b6-488f-a4b6-b2da8b769e06
Distribution End Date
2017-11-30

Device Description

CANNULA CB96021 FEM 21ART 21VEN

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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

GMDN Terms

Code Name
47733 Cardiopulmonary bypass cannula, femoral

Identifiers

Type ID
Primary 00673978864921

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K875353 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 21 FR Venous
Device Size Text, specify 21 FR Arterial

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 40 Degrees Celsius