FDA UDI Not in Commercial Distribution 🇺🇸 United States

Intersept®

DI: 00613994352828 · Model: 6125 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Intersept®
Primary DI
00613994352828
Version / Model
6125
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-22
Public Version
5
Public Version Date
2023-05-18
Public Version Status
Update
Public Device Record Key
ffd89bb4-9b2d-4dcb-869d-e3361112e981
Distribution End Date
2019-05-02

Device Description

CONN 6125 1/2X1/2 STRAIGHT 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
Yes
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
DTL Adaptor, stopcock, manifold, fitting, cardiopulmonary bypass

GMDN Terms

Code Name
35441 Cardiopulmonary bypass system blood tubing set

Identifiers

Type ID
Package 20673978555267
Primary 00613994352828

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 12.7 MM Port Outer Diameter