FDA UDI In Commercial Distribution 🇺🇸 United States

CARPENTIER-EDWARDS PHYSIO II ANNULOPLASTY RING

DI: 00690103180220 · Model: 5200 · Edwards Lifesciences LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CARPENTIER-EDWARDS PHYSIO II ANNULOPLASTY RING
Primary DI
00690103180220
Version / Model
5200
Catalog Number
5200M34
Company Name
Edwards Lifesciences LLC
Labeler DUNS
134139174
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
6
Public Version Date
2023-08-14
Public Version Status
Update
Public Device Record Key
ac6b5697-ad50-4146-8fe7-70e3d1a3b5cf

Device Description

CARPENTIER-EDWARDS PHYSIO II ANNULOPLASTY RING

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
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
KRH RING, ANNULOPLASTY

GMDN Terms

Code Name
66338 Mitral/tricuspid annuloplasty ring, open-surgery

Identifiers

Type ID
Primary 00690103180220

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K083470 000

Device Sizes

Type Value Unit Text
Device Size Text, specify MEASUREMENT OF THE INTER-COMMISSURAL DISTANCE AND HEIGHT AND/OR SURFACE AREA 34 MILLIMETERS

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
STORE IN DRY LOCATION