FDA UDI In Commercial Distribution 🇺🇸 United States

Libertas

DI: 00810008120002 · Model: MO-MSEC-40/MA · MAXX ORTHOPEDICS, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Libertas
Primary DI
00810008120002
Version / Model
MO-MSEC-40/MA
Company Name
MAXX ORTHOPEDICS, INC.
Labeler DUNS
792030103
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-09
Public Version
1
Public Version Date
2022-12-19
Public Version Status
New
Public Device Record Key
8bc09f70-1900-44b0-a7cb-b7942a2d0761

Device Description

Modular Shell Size 40/MA - 2 Holes

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
LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented
JDI Prosthesis, hip, semi-constrained, metal/polymer, cemented

GMDN Terms

Code Name
43168 Non-constrained polyethylene acetabular liner

Identifiers

Type ID
Primary 00810008120002

Premarket Submissions

Submission Number Supplement Number
K180973 000