FDA UDI In Commercial Distribution 🇺🇸 United States

EVOLUTION

DI: M684E15000201 · Model: E1500020 · Microport Orthopedics Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EVOLUTION
Primary DI
M684E15000201
Version / Model
E1500020
Catalog Number
E1500020
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
4
Public Version Date
2023-10-04
Public Version Status
Update
Public Device Record Key
bb929fce-8099-41f7-a97d-33231db0aa30

Device Description

EVOLUTION® KA EM TIBIAL SHIM UNIVERSAL

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
FZX Guide, surgical, instrument

GMDN Terms

Code Name
45114 Bone-resection orthopaedic reamer, reusable

Identifiers

Type ID
Primary M684E15000201

Customer Contacts