FDA UDI In Commercial Distribution 🇺🇸 United States

EVOLUTION

DI: M684E21020091 · Model: E2102009 · Microport Orthopedics Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EVOLUTION
Primary DI
M684E21020091
Version / Model
E2102009
Catalog Number
E2102009
Company Name
Microport Orthopedics Inc.
Labeler DUNS
079118736
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-12-23
Public Version
1
Public Version Date
2019-12-31
Public Version Status
New
Public Device Record Key
1b0d92c3-b9ea-4f30-ab3e-bdb123d20c7c

Device Description

EVOLUTION® KA TIBIA EM ANKLE CLAMP ASSEMBLY

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
Yes
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
HXD CLAMP

GMDN Terms

Code Name
59009 Orthopaedic implant/instrument assembling device

Identifiers

Type ID
Primary M684E21020091

Customer Contacts