FDA UDI In Commercial Distribution 🇺🇸 United States

Intersept®

DI: 00673978555409 · Model: 6161 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Intersept®
Primary DI
00673978555409
Version / Model
6161
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-23
Public Version
4
Public Version Date
2022-12-08
Public Version Status
Update
Public Device Record Key
d3e3e7c1-c7a6-401f-9b59-16b341389a1b

Device Description

CONN 6161 1/4X1/4 W/LL PRT&PLG BULK 20PK

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
No
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
DWE TUBING, PUMP, CARDIOPULMONARY BYPASS

GMDN Terms

Code Name
35441 Cardiopulmonary bypass system blood tubing set

Identifiers

Type ID
Package 20673978555403
Primary 00673978555409

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K800178 000