FDA UDI In Commercial Distribution 🇺🇸 United States

Bio-Medicus®

DI: 00613994530707 · Model: 96820-008 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Bio-Medicus®
Primary DI
00613994530707
Version / Model
96820-008
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-24
Public Version
4
Public Version Date
2024-06-19
Public Version Status
Update
Public Device Record Key
c0d1358b-e7a4-472b-9d14-b349e1448e0f

Device Description

CANNULA 96820-008 BIO-MED ART 8FR EA 17L

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
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 00613994530707

Customer Contacts

Device Sizes

Type Value Unit Text
Catheter Gauge 8.0 French
Length 10.0 Centimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Do not store Carmeda® coated product over 40° C.