FDA UDI In Commercial Distribution 🇺🇸 United States

DLP™

DI: 00763000193010 · Model: CB87022 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DLP™
Primary DI
00763000193010
Version / Model
CB87022
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-06
Public Version
2
Public Version Date
2022-08-05
Public Version Status
Update
Public Device Record Key
c6c78833-3a18-479e-a8df-b316ad514e17

Device Description

CANNULA CB87022 ART CUR TIP 22FR

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, arterial

Identifiers

Type ID
Primary 00763000193010

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K840002 000

Device Sizes

Type Value Unit Text
Catheter Gauge 22.0 French

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store the product at room temperature.
Type
Handling Environment Temperature
Temperature Range
– 40 Degrees Celsius