FDA UDI In Commercial Distribution 🇺🇸 United States

Profemur

DI: M684PPW380461 · Model: PPW38046 · Microport Orthopedics Inc.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Profemur
Primary DI
M684PPW380461
Version / Model
PPW38046
Catalog Number
PPW38046
Company Name
Microport Orthopedics Inc.
Labeler DUNS
079118736
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-31
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
145aece1-86dd-4d87-99a8-b40aba3e9dcf

Device Description

PROFEMUR 215MM STEM BOWED/TAPER SIZE 16

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
MR Conditional
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
MRA Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented
LWJ Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented

GMDN Terms

Code Name
55833 Press-fit hip femur prosthesis, modular

Identifiers

Type ID
Direct Marking PPW38046
Primary M684PPW380461

Customer Contacts

Device Sizes

Type Value Unit Text
Length 215 Millimeter