FDA UDI In Commercial Distribution 🇺🇸 United States

PROFEMUR®

DI: M684PRFC00131 · Model: PRFC0013 · Microport Orthopedics Inc.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
PROFEMUR®
Primary DI
M684PRFC00131
Version / Model
PRFC0013
Catalog Number
PRFC0013
Company Name
Microport Orthopedics Inc.
Labeler DUNS
079118736
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-20
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
8e18067f-0db2-4f7b-8b23-da4c002ecef4

Device Description

PROFEMUR® FC STEM SZ 13

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
MBL Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous
LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

GMDN Terms

Code Name
34191 Coated femoral stem prosthesis, modular

Identifiers

Type ID
Direct Marking PRFC0013
Primary M684PRFC00131

Customer Contacts