Polysulfide dental impression material - UK MHRA Medical Device Registration

Polysulfide dental impression material is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 123390. The device is manufactured by Howmedica Osteonics Corp. from United States, classified as General Medical Device. The authorized representative in the UK is Stryker UK Ltd.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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Polysulfide dental impression material

MHRA Device ID: 123390•Ref: 123390

Device Type

General Medical Device

Devices

Polysulfide dental impression material

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Dec 28, 2023

Manufacturer Information

Name

Howmedica Osteonics Corp.

Address

325 Corporate Drive

Mahwah, New Jersey, United States

Created Date

Mar 26, 2021

Authorized Representative

Name

Stryker UK Ltd

Relationship Type

UK Responsible Person

Address

Stryker House Hambridge Road

Newbury, Berkshire, England, United Kingdom

Postcode: RG14 5AW

DJ Fang

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Other Products from Howmedica Osteonics Corp. (10)

Other Products from Same Authorized Representative (10)

Polysulfide dental impression material - UK MHRA Medical Device Registration

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Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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