FDA UDI In Commercial Distribution 🇺🇸 United States

CARPENTIER-EDWARDS PERIMOUNT BIOPROSTHESIS AORTIC

DI: 00690103162271 · Model: 3000 · Edwards Lifesciences LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CARPENTIER-EDWARDS PERIMOUNT BIOPROSTHESIS AORTIC
Primary DI
00690103162271
Version / Model
3000
Catalog Number
300027MM
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
c97887b5-3599-4917-8086-1d32b351009e

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 00690103162271

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P860057 018
P860057 019
P860057 022
P860057 023
P860057 030
P860057 036
P860057 037
P860057 039
P860057 041
P860057 045
P860057 051
P860057 053
P860057 062
P860057 100
P860057 152

Device Sizes

Type Value Unit Text
Device Size Text, specify STENT DIAMETER (WIREFORM), 27 MILLIMETER

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
10 – 25 Degrees Celsius