FDA UDI In Commercial Distribution 🇺🇸 United States

PRIME

DI: M684P2LXFD361 · Model: P2LXFD36 · Microport Orthopedics Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PRIME
Primary DI
M684P2LXFD361
Version / Model
P2LXFD36
Catalog Number
P2LXFD36
Company Name
Microport Orthopedics Inc.
Labeler DUNS
079118736
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-07-30
Public Version
1
Public Version Date
2018-08-30
Public Version Status
New
Public Device Record Key
48c81bb9-a560-426b-a2cb-0e198996f278

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
LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, 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 M684P2LXFD361

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K180798 000

Device Sizes

Type Value Unit Text
Outer Diameter 36 Millimeter