FDA UDI Not in Commercial Distribution 🇺🇸 United States

Bio-Medicus®

DI: 00613994504715 · Model: 98000-158 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Bio-Medicus®
Primary DI
00613994504715
Version / Model
98000-158
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-24
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
8b4d2f41-3c79-4176-98be-3822a2b5aef8
Distribution End Date
2017-11-30

Device Description

CANNULA 98000-158 BIO-MED ART 19 O/HOLE

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
47733 Cardiopulmonary bypass cannula, femoral

Identifiers

Type ID
Primary 00613994504715

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K924642 000

Device Sizes

Type Value Unit Text
Length 15.0 Centimeter
Catheter Gauge 19.0 French

Storage Conditions

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