FDA UDI In Commercial Distribution 🇺🇸 United States

ADVANCE®

DI: M684KIPSS5121 · Model: KIPSS512 · Microport Orthopedics Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ADVANCE®
Primary DI
M684KIPSS5121
Version / Model
KIPSS512
Catalog Number
KIPSS512
Company Name
Microport Orthopedics Inc.
Labeler DUNS
079118736
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-03-02
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
4a42ace2-42d9-4669-a934-96963f02e31f

Device Characteristics

Single Use
No
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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HWT TEMPLATE

GMDN Terms

Code Name
44742 Joint prosthesis implantation kit, reusable

Identifiers

Type ID
Primary M684KIPSS5121

Customer Contacts