FDA UDI In Commercial Distribution 🇺🇸 United States

Libertas

DI: 00810008124604 · Model: MO-MLLH-MJ/40 · MAXX ORTHOPEDICS, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Libertas
Primary DI
00810008124604
Version / Model
MO-MLLH-MJ/40
Company Name
MAXX ORTHOPEDICS, INC.
Labeler DUNS
792030103
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-08
Public Version
1
Public Version Date
2022-12-16
Public Version Status
New
Public Device Record Key
41900193-0001-42db-a15d-0acfb1c90c1b

Device Description

Modular E-XLPE Liner Size MJ/40 Elevated Wall

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
OQI Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented
OQG Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented
LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented

GMDN Terms

Code Name
43168 Non-constrained polyethylene acetabular liner

Identifiers

Type ID
Primary 00810008124604

Premarket Submissions

Submission Number Supplement Number
K192989 000