FDA UDI In Commercial Distribution 🇺🇸 United States

ORTHOSET®

DI: M684141010001 · Model: 14101000 · Microport Orthopedics Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ORTHOSET®
Primary DI
M684141010001
Version / Model
14101000
Catalog Number
14101000
Company Name
Microport Orthopedics Inc.
Labeler DUNS
079118736
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
3
Public Version Date
2020-06-19
Public Version Status
Update
Public Device Record Key
db09fbff-b881-40ad-988c-974267a1e479

Device Description

ORTHOSET® I BONE CEMENT

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
LOD Bone Cement

GMDN Terms

Code Name
35217 Orthopaedic cement, non-antimicrobial

Identifiers

Type ID
Direct Marking 14101000
Primary M684141010001

Customer Contacts