FDA UDI In Commercial Distribution 🇺🇸 United States

Evolution Revision CCK System

DI: M684E60010111 · Model: E6001011 · Microport Orthopedics Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Evolution Revision CCK System
Primary DI
M684E60010111
Version / Model
E6001011
Catalog Number
E6001011
Company Name
Microport Orthopedics Inc.
Labeler DUNS
079118736
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-04-02
Public Version
2
Public Version Date
2018-07-06
Public Version Status
New
Public Device Record Key
94fd4f72-2770-4cc4-8e19-36cbc93bdd64

Device Characteristics

Single Use
No
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
No
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
PBF Orthopaedic surgical planning and instrument guides

GMDN Terms

Code Name
44742 Joint prosthesis implantation kit, reusable

Identifiers

Type ID
Primary M684E60010111

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K171389 000