FDA UDI In Commercial Distribution 🇺🇸 United States

ORTHOLOC®

DI: M684185001561 · Model: 18500156 · Microport Orthopedics Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ORTHOLOC®
Primary DI
M684185001561
Version / Model
18500156
Catalog Number
18500156
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
2bfa7820-6f79-4f87-be52-1b9626d500b1

Device Description

ORTHOLOC® II POST STAB TIBIAL INSERT THICK XLG 16mm

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
Labeling does not contain MRI Safety Information
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
HRY Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer

GMDN Terms

Code Name
33665 Posterior-stabilized total knee prosthesis

Identifiers

Type ID
Direct Marking 18500156
Primary M684185001561

Customer Contacts

Device Sizes

Type Value Unit Text
Height 16 Millimeter