Bone access cannula - UK MHRA Medical Device Registration

Bone access cannula is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 93043. The device is manufactured by Invivo Corporation from United States, classified as General Medical Device. The authorized representative in the UK is Philips Electronics 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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Bone access cannula

MHRA Device ID: 93043•Ref: 93043

Device Type

General Medical Device

Devices

Bone access cannula

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

May 21, 2024

Manufacturer Information

Name

Invivo Corporation

Address

3545 SW 47th Avenue

Gainesville, Florida, United States

Created Date

Aug 7, 2021

Authorized Representative

Name

Philips Electronics UK Ltd

Relationship Type

UK Responsible Person

Address

Ascent 1 Farnborough Aerospace Centre

Farnborough, Hampshire, England, United Kingdom

Postcode: GU14 6XW

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Bone access cannula - UK MHRA Medical Device Registration

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Date Registered

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Created Date

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Address

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