FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 00763000185107 · Model: 10R68R · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00763000185107
Version / Model
10R68R
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-19
Public Version
3
Public Version Date
2023-11-22
Public Version Status
Update
Public Device Record Key
0f7f6cda-c771-42f0-8cd1-175a7baa8bb9
Distribution End Date
2023-11-01

Device Description

CUSTOM PACK 10R68R 10PK MYOTHRM SUPP

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
DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass

GMDN Terms

Code Name
35441 Cardiopulmonary bypass system blood tubing set

Identifiers

Type ID
Package 20763000185118
Primary 00763000185107

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K171308 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 50 Degrees Celsius