FDA UDI In Commercial Distribution 🇺🇸 United States

ORTHOLOC®

DI: M684187110071 · Model: 18711007 · Microport Orthopedics Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ORTHOLOC®
Primary DI
M684187110071
Version / Model
18711007
Catalog Number
18711007
Company Name
Microport Orthopedics Inc.
Labeler DUNS
079118736
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-02-13
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
1305c5b3-6888-4196-81a3-ee9bc795faa7

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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
44742 Joint prosthesis implantation kit, reusable

Identifiers

Type ID
Primary M684187110071

Customer Contacts