← Back to catalogue

Metafix Hip Stem

FDA UDI

Class II (US FDA UDI)

by Corin Ltd

Identity

Trade Name
Metafix Hip Stem FDA UDI
Generic Name
Orthopaedic broach FDA UDI
Device Name
Size 3 Femoral Broach FDA UDI
Model / Reference
340.433H FDA UDI
Description
Size 3 Femoral Broach FDA UDI

Identifiers

Primary DI / UDI-DI
05055343891599 FDA UDI
510(k) Number
K153381 FDA UDI
FDA Product Code
MEH FDA UDI
OQI FDA UDI
JDI FDA UDI
KWY FDA UDI
KWL FDA UDI
LZO FDA UDI
GMDN Term
Orthopaedic broach FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3353 FDA UDI
888.3350 FDA UDI
888.3390 FDA UDI
888.3360 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: Orthopaedic broach

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

Similar devices

Also classified as Orthopaedic broach.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Corin Ltd

Sources (1)

  • FDA UDI 76329dd0-65ea-48ce-aa16-b82cf7844b1d 34 fields · synced May 30, 2026