FDA UDI In Commercial Distribution 🇺🇸 United States

INSPIRIS RESILIA AORTIC VALVE

DI: 00690103195002 · Model: 11500A · Edwards Lifesciences LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
INSPIRIS RESILIA AORTIC VALVE
Primary DI
00690103195002
Version / Model
11500A
Catalog Number
11500A27
Company Name
Edwards Lifesciences LLC
Labeler DUNS
134139174
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-07-31
Public Version
6
Public Version Date
2023-01-05
Public Version Status
Update
Public Device Record Key
84457b71-0469-489c-885b-eed8412b2924

Device Description

INSPIRIS RESILIA AORTIC VALVE

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
Yes
Has Donation ID
Yes

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 00690103195002

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P150048 000
P150048 060

Device Sizes

Type Value Unit Text
Device Size Text, specify 27MM

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
10 – 25 Degrees Celsius