FDA UDI In Commercial Distribution 🇺🇸 United States

DLP™

DI: 00643169697454 · Model: CB68136 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
DLP™
Primary DI
00643169697454
Version / Model
CB68136
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
5
Public Version Date
2024-06-19
Public Version Status
Update
Public Device Record Key
6dc53a25-7dd6-428b-a91e-5b6ad57af0f7

Device Description

CANN CB68136 SS VEN MAL 36F 17

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
34893 Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, return

Identifiers

Type ID
Primary 00643169697454

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K033264 000

Device Sizes

Type Value Unit Text
Catheter Gauge 36.0 French

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 40 Degrees Celsius