FDA UDI Not in Commercial Distribution 🇺🇸 United States

Custom Perfusion System

DI: 00643169593541 · Model: TL7P15R11 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Custom Perfusion System
Primary DI
00643169593541
Version / Model
TL7P15R11
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-02-18
Public Version
5
Public Version Date
2022-12-08
Public Version Status
Update
Public Device Record Key
75812876-5084-4769-9b86-a4a74caeb1b7
Distribution End Date
2015-10-21

Device Description

CUSTOM PACK TL7P15R11 SPRINGDL

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
Yes
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 00643169593541

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K973011 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 50 Degrees Celsius