Suture knot pusher, single-use - UK MHRA Medical Device Registration

Suture knot pusher, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 100426. The device is manufactured by Stryker Endoscopy, a division of Stryker Corporation 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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Suture knot pusher, single-use

MHRA Device ID: 100426•Ref: 100426

Device Type

General Medical Device

Devices

Suture knot pusher, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Dec 21, 2023

Manufacturer Information

Name

Stryker Endoscopy, a division of Stryker Corporation

Address

5900 Optical Ct

San Jose, United States

Created Date

Mar 17, 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

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Suture knot pusher, single-use - UK MHRA Medical Device Registration

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Date Registered

Last Updated

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Created Date

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