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Corin Bipolar Prosthesis

FDA UDI

Class II (US FDA UDI)

by Corin Ltd

Identity

Trade Name
Corin Bipolar Prosthesis FDA UDI
Generic Name
Femoral head prosthesis trial FDA UDI
Device Name
BIPOLAR EUROCONE TRIAL HEAD 40mm LONG FDA UDI
Model / Reference
E211.940 FDA UDI
Description
BIPOLAR EUROCONE TRIAL HEAD 40mm LONG FDA UDI

Identifiers

Catalog Number
E211.940 FDA UDI
Primary DI / UDI-DI
05055196948464 FDA UDI
510(k) Number
K925897 FDA UDI
FDA Product Code
KWY FDA UDI
GMDN Term
Femoral head prosthesis trial FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3390 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Femoral head prosthesis trial

Corin Bipolar Prosthesis by Corin Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Femoral head prosthesis trial.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Corin Ltd

Sources (1)

  • FDA UDI d579f02d-d544-481b-95ca-65c0b3780db2 36 fields · synced May 31, 2026