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Evolution

FDA UDI

Class II (US FDA UDI)

by MicroPort Orthopedics Inc.

Identity

Trade Name
Evolution FDA UDI
Generic Name
Joint prosthesis implantation kit, reusable FDA UDI
Device Name
EVOLUTION REV CONICAL BROACH SIZE 3 FDA UDI
Model / Reference
E223CN03 FDA UDI
Description
EVOLUTION REV CONICAL BROACH SIZE 3 FDA UDI

Identifiers

Catalog Number
E223CN03 FDA UDI
Primary DI / UDI-DI
00192629408722 FDA UDI
510(k) Number
K233507 FDA UDI
FDA Product Code
JWH FDA UDI
KRO FDA UDI
MBH FDA UDI
GMDN Term
Joint prosthesis implantation kit, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3560 FDA UDI
888.3510 FDA UDI
888.3565 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Joint prosthesis implantation kit, reusable

Evolution by MicroPort Orthopedics Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Joint prosthesis implantation kit, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2f6c9ba2-e52d-4267-bba5-e1acfbbfdd0b 35 fields · synced Jun 9, 2026