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Centrax

FDA UDI

Class II (US FDA UDI)

by Howmedica Osteonics Corp.

Identity

Trade Name
Centrax FDA UDI
Generic Name
Bipolar femoral head outer component, hemiarthroplasty FDA UDI
Device Name
Bipolar Duration Stabilized FDA UDI
Model / Reference
6226-2-248 FDA UDI
Description
Bipolar Duration Stabilized FDA UDI

Identifiers

Catalog Number
6226-2-248 FDA UDI
Primary DI / UDI-DI
07613327032062 FDA UDI
510(k) Number
K972792 FDA UDI
FDA Product Code
JDI FDA UDI
KWY FDA UDI
GMDN Term
Bipolar femoral head outer component, hemiarthroplasty FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3350 FDA UDI
888.3390 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Lumen/Inner Diameter — 22.0 Millimeter FDA UDI
Outer Diameter — 48.0 Millimeter FDA UDI

Category: Bipolar femoral head outer component, hemiarthroplasty

Centrax by Howmedica Osteonics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bipolar femoral head outer component, hemiarthroplasty.

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 ff47d29a-49f1-4ce3-b34e-846304e0d053 36 fields · synced May 30, 2026