FDA UDI In Commercial Distribution 🇺🇸 United States

Intersept® Custom Tubing Pack

DI: 00643169118560 · Model: 5Z93R5 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Intersept® Custom Tubing Pack
Primary DI
00643169118560
Version / Model
5Z93R5
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-23
Public Version
4
Public Version Date
2022-12-08
Public Version Status
Update
Public Device Record Key
d41da4f7-9b97-4a98-ae96-d9403a822ad1

Device Description

CUSTOM PACK 5Z93R5 BIO PUMP PK

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
KFM PUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE

GMDN Terms

Code Name
35441 Cardiopulmonary bypass system blood tubing set

Identifiers

Type ID
Primary 00643169118560

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K973011 000