Balloon kyphoplasty kit - UK MHRA Medical Device Registration

Balloon kyphoplasty kit is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 98345. The device is manufactured by Globus Medical, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is AJW Technology Consulting 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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Balloon kyphoplasty kit

MHRA Device ID: 98345•Ref: 98345

Device Type

General Medical Device

Devices

Balloon kyphoplasty kit

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Jan 16, 2024

Manufacturer Information

Name

Globus Medical, Inc.

Address

2560 General Armistead Avenue

Audubon, United States

Created Date

Apr 14, 2021

Authorized Representative

Name

AJW Technology Consulting Ltd

Relationship Type

UK Responsible Person

Address

4/4a Bloomsbury Square

London, England, United Kingdom

Postcode: WC1A 2RP

DJ Fang

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Other Products from Globus Medical, Inc. (10)

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Balloon kyphoplasty kit - UK MHRA Medical Device Registration

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Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

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DJ Fang

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