FDA UDI In Commercial Distribution 🇺🇸 United States

Open Pivot™

DI: 00643169335080 · Model: 500FA19 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Open Pivot™
Primary DI
00643169335080
Version / Model
500FA19
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
2021-02-05
Public Version Status
Update
Public Device Record Key
533a9e2d-e16b-4526-abeb-cbad3e561e16

Device Description

MHV 500FA19 STD AORTIC

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LWQ HEART-VALVE, MECHANICAL

GMDN Terms

Code Name
60240 Aortic bi-leaflet mechanical heart valve prosthesis

Identifiers

Type ID
Primary 00643169335080

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P990046 003

Device Sizes

Type Value Unit Text
Device Size Text, specify Tissue Annulus 19 MM

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 50 Degrees Celsius