FDA UDI In Commercial Distribution 🇺🇸 United States

PROFEMUR®

DI: 00192629013605 · Model: PPW38073 · Microport Orthopedics Inc.
Product Codes
3
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PROFEMUR®
Primary DI
00192629013605
Version / Model
PPW38073
Catalog Number
PPW38073
Company Name
Microport Orthopedics Inc.
Labeler DUNS
079118736
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-02-16
Public Version
1
Public Version Date
2022-02-24
Public Version Status
New
Public Device Record Key
120c2347-7688-44b9-9c3f-2ba38d095b58

Device Description

PROFEMUR® PROX BODY RASP STD 3

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
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED
JDI Prosthesis, hip, semi-constrained, metal/polymer, cemented
LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented

GMDN Terms

Code Name
44742 Joint prosthesis implantation kit, reusable

Identifiers

Type ID
Secondary M684PPW380731
Primary 00192629013605

Customer Contacts