FDA UDI In Commercial Distribution 🇺🇸 United States

CARPENTIER-EDWARDS S.A.VBIOPROSTHESIS - AORTIC

DI: 00690103146905 · Model: 2650 · Edwards Lifesciences LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CARPENTIER-EDWARDS S.A.VBIOPROSTHESIS - AORTIC
Primary DI
00690103146905
Version / Model
2650
Catalog Number
265027MM
Company Name
Edwards Lifesciences LLC
Labeler DUNS
134139174
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-08-30
Public Version
4
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
a1866822-cf77-4099-a675-5fb8a6ac40b9

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DYE replacement Heart-valve

GMDN Terms

Code Name
60242 Aortic heart valve bioprosthesis

Identifiers

Type ID
Primary 00690103146905

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P010041 002
P010041 009
P010041 012
P010041 015
P010041 040

Device Sizes

Type Value Unit Text
Device Size Text, specify MOUNTING DIAMETER (ANNULUS), 27 MILLIMETER

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
10 – 25 Degrees Celsius