FDA UDI In Commercial Distribution 🇺🇸 United States

Open Pivot™

DI: 00643169977792 · Model: 500FA21 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Open Pivot™
Primary DI
00643169977792
Version / Model
500FA21
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-01-14
Public Version
2
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
8f3eb523-e635-42d2-b1c1-dd1efb893a5d

Device Description

MHV 500FA21 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 00643169977792

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P990046 000

Device Sizes

Type Value Unit Text
Lumen/Inner Diameter 21.0 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
The storage environment should be clean, cool, and dry.