FDA UDI In Commercial Distribution 🇺🇸 United States

CARPENTIER-EDWARDS PERIMOUNT MAGNA EASE PERICARDIAL BIOPROSTHESIS - AORTIC

DI: 00690103176124 · Model: 3300TFX · Edwards Lifesciences LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CARPENTIER-EDWARDS PERIMOUNT MAGNA EASE PERICARDIAL BIOPROSTHESIS - AORTIC
Primary DI
00690103176124
Version / Model
3300TFX
Catalog Number
3300TFX19MM
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
7
Public Version Date
2022-01-19
Public Version Status
Update
Public Device Record Key
6f6e1b79-6cfb-49ce-80fa-40d22327da4c

Device Description

CARPENTIER-EDWARDS PERIMOUNT MAGNA EASE PERICARDIAL AORTIC BIOPROSTHESIS

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
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 00690103176124

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P860057 042
P860057 045
P860057 051
P860057 053
P860057 100
P860057 152
P860057 203

Device Sizes

Type Value Unit Text
Device Size Text, specify STENT DIAMETER, (TAD), 19 MILLIMETER

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
10 – 25 Degrees Celsius