FDA UDI Not in Commercial Distribution 🇺🇸 United States

DLP®

DI: 00643169160224 · Model: CB67518 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DLP®
Primary DI
00643169160224
Version / Model
CB67518
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-22
Public Version
5
Public Version Date
2022-09-13
Public Version Status
Update
Public Device Record Key
fef353eb-0a89-47a6-ba42-7152f6c414ec
Distribution End Date
2021-06-23

Device Description

CANN CB67518 VEN RT PVC 18F 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
34905 Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, venous

Identifiers

Type ID
Primary 00643169160224

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K840001 000

Device Sizes

Type Value Unit Text
Catheter Gauge 18.0 French

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 40 Degrees Celsius