Spinal procedural guidewire - UK MHRA Medical Device Registration

Spinal procedural guidewire is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 71925. The device is manufactured by Abbott Medical from United States, classified as Active implantable device (Directive 90/385/EEC only). The authorized representative in the UK is Abbott Medical UK Limited.

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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MHRA Registered

Active implantable device (Directive 90/385/EEC only)

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Spinal procedural guidewire

MHRA Device ID: 71925

Device Type

Active implantable device (Directive 90/385/EEC only)

Devices

Spinal procedural guidewire

Type

Active implantable Medical device

Date Registered

Mar 12, 2021

Last Updated

Dec 22, 2022

Manufacturer Information

Name

Abbott Medical

Address

6901 Preston Road

Plano, Texas, United States

Created Date

Mar 12, 2021

Authorized Representative

Name

Abbott Medical UK Limited

Relationship Type

UK Responsible Person

Address

Elder House Central Boulevard Blythe Valley Business Park

Solihull, West Midlands, England, United Kingdom

Postcode: B90 8AJ

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Spinal procedural guidewire - UK MHRA Medical Device Registration

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Devices

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Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

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Spinal procedural guidewire

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