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Howmedica, Definition

FDA UDI

Class I (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
Howmedica, Definition FDA UDI
Generic Name
Orthopaedic cement/bone filler dispensing gun FDA UDI
Device Name
Femoral Pressuring Seal Size 1-4 FDA UDI
Model / Reference
6265004301 FDA UDI
Description
Femoral Pressuring Seal Size 1-4 FDA UDI

Identifiers

Catalog Number
6265004301 FDA UDI
Primary DI / UDI-DI
04546540263179 FDA UDI
FDA Product Code
JDZ FDA UDI
GMDN Term
Orthopaedic cement/bone filler dispensing gun FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4210 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthopaedic cement/bone filler dispensing gun

Howmedica, Definition by Stryker Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic cement/bone filler dispensing gun.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 9f61467f-4aca-4339-b219-38ffb8a390dd 36 fields · synced May 30, 2026