Cranial bur, single-use - UK MHRA Medical Device Registration

Cranial bur, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 160171. The device is manufactured by The Anspach Effort INC. from United States, classified as General Medical Device. The authorized representative in the UK is Johnson & Johnson Medical 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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Cranial bur, single-use

MHRA Device ID: 160171•Ref: 160171

Device Type

General Medical Device

Devices

Cranial bur, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Sep 7, 2024

Manufacturer Information

Name

The Anspach Effort INC.

Address

4500 Riverside Drive Riverside Dr Palm Beach Gardens

Palm Beach, FL, United States

Created Date

Jun 25, 2021

Authorized Representative

Name

Johnson & Johnson Medical Ltd

Relationship Type

UK Responsible Person

Address

Baird House 4 Lower Gilmore Bank

Edinburgh, Scotland, United Kingdom

Postcode: EH3 9QP

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Other Products from The Anspach Effort INC. (10)

Other Products from Same Authorized Representative (10)

Cranial bur, single-use - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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