FDA UDI In Commercial Distribution 🇺🇸 United States

Avalus™

DI: 00643169983199 · Model: 40023 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Avalus™
Primary DI
00643169983199
Version / Model
40023
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-11-21
Public Version
5
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
39559a3d-72f3-4089-9e44-b4c6efacaee0

Device Description

VALVE 40023 AVALUS AOR MMX U30 US

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 Safe
Direct Marking Exempt
Yes
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
LWR heart-valve, non-allograft tissue

GMDN Terms

Code Name
60242 Aortic heart valve bioprosthesis

Identifiers

Type ID
Primary 00643169983199

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P170006 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Valve Size 23 MM

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Do not expose the valve to sunlight or other ultraviolet light sources, or placed where significant temperature fluctuations could occur.
Type
Storage Environment Temperature
Temperature Range
5 – 25 Degrees Celsius