FDA UDI In Commercial Distribution 🇺🇸 United States

DLP™

DI: 00763000192846 · Model: CB77012 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DLP™
Primary DI
00763000192846
Version / Model
CB77012
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
33f35aaf-4d98-4f2e-9d5f-9171261f26f0

Device Description

CANN CB77012 ART ONE PIECE 12FR 17L

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 00763000192846

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K840001 000

Device Sizes

Type Value Unit Text
Catheter Gauge 12.0 French

Storage Conditions

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