Atherectomy laser system beam guide-catheter, peripheral - UK MHRA Medical Device Registration

Atherectomy laser system beam guide-catheter, peripheral is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 97242. The device is manufactured by Spectranetics Corporation - Colorado Springs 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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Atherectomy laser system beam guide-catheter, peripheral

MHRA Device ID: 97242•Ref: 97242

Device Type

General Medical Device

Devices

Atherectomy laser system beam guide-catheter, peripheral

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Feb 1, 2024

Manufacturer Information

Name

Spectranetics Corporation - Colorado Springs

Address

9965 Federal Drive

Colorado Springs, United States

Created Date

Apr 26, 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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Other Products from Spectranetics Corporation - Colorado Springs (10)

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Atherectomy laser system beam guide-catheter, peripheral - 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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