FDA UDI In Commercial Distribution 🇺🇸 United States

ADVANCE®

DI: M684KIRV314M1 · Model: KIRV314M · Microport Orthopedics Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ADVANCE®
Primary DI
M684KIRV314M1
Version / Model
KIRV314M
Catalog Number
KIRV314M
Company Name
Microport Orthopedics Inc.
Labeler DUNS
079118736
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-20
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
caf2d643-87c8-4b89-8ab9-4d415521032f

Device Description

ADVANCE® II REVISION CCK INSERT SIZE 3 MINUS 14mm

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
No
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
JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

GMDN Terms

Code Name
33665 Posterior-stabilized total knee prosthesis

Identifiers

Type ID
Direct Marking KIRV314M
Primary M684KIRV314M1

Customer Contacts

Device Sizes

Type Value Unit Text
Height 14 Millimeter