FDA UDI In Commercial Distribution 🇺🇸 United States

Perfecta

DI: M684378710501 · Model: 37871050 · Microport Orthopedics Inc.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Perfecta
Primary DI
M684378710501
Version / Model
37871050
Catalog Number
37871050
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
4ceea71d-190e-46be-90c8-521969184c62

Device Description

PERFECTA PLASMA SPRAYED FEMORAL STEM SZ 10.5 RDC FLARE

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
JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

GMDN Terms

Code Name
55833 Press-fit hip femur prosthesis, modular

Identifiers

Type ID
Direct Marking 37871050
Primary M684378710501

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 10.5 Millimeter