FDA UDI In Commercial Distribution 🇺🇸 United States

EVOLUTION

DI: 00192629276598 · Model: E1200045 · Microport Orthopedics Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
EVOLUTION
Primary DI
00192629276598
Version / Model
E1200045
Catalog Number
E1200045
Company Name
Microport Orthopedics Inc.
Labeler DUNS
079118736
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-05-20
Public Version
1
Public Version Date
2025-05-28
Public Version Status
New
Public Device Record Key
ea008e9b-8a03-4488-8c8e-f43f1cc03871

Device Description

EVOLUTION FEM SIZING TEMPLATE A/P SIZE 4/5

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
KRO PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER

GMDN Terms

Code Name
44742 Joint prosthesis implantation kit, reusable

Identifiers

Type ID
Secondary M684E12000451
Primary 00192629276598

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K230563 000