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Revival Modular Hip Stem

FDA UDI

Class II (US FDA UDI)

by Corin Ltd

Identity

Trade Name
Revival Modular Hip Stem FDA UDI
Generic Name
Revision uncoated hip femur prosthesis FDA UDI
Device Name
Distal Component 240mm Length; 21mm Diameter FDA UDI
Model / Reference
120376021 FDA UDI
Description
Distal Component 240mm Length; 21mm Diameter FDA UDI

Identifiers

Primary DI / UDI-DI
08033466132154 FDA UDI
FDA Product Code
MEH FDA UDI
LZO FDA UDI
GMDN Term
Revision uncoated hip femur prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3353 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Revision uncoated hip femur prosthesis

Revival Modular Hip Stem by Corin Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Revision uncoated hip femur prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Corin Ltd

Sources (1)

  • FDA UDI 18f223d2-7f86-4008-a86d-494e0267ca25 33 fields · synced May 30, 2026