Soft-tissue biopsy procedure kit, non-medicated - UK MHRA Medical Device Registration

Soft-tissue biopsy procedure kit, non-medicated is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 139553. The device is manufactured by SenoRx, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is Becton, Dickinson U.K. 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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Soft-tissue biopsy procedure kit, non-medicated

MHRA Device ID: 139553•Ref: 139553

Device Type

General Medical Device

Devices

Soft-tissue biopsy procedure kit, non-medicated

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Mar 23, 2024

Manufacturer Information

Name

SenoRx, Inc.

Address

1625 W 3rd Street

Tempe, Arizona, United States

Created Date

Mar 19, 2021

Authorized Representative

Name

Becton, Dickinson U.K. Limited

Relationship Type

UK Responsible Person

Address

1030 Eskdale Road Winnersh Triangle, Wokingham

Winnersh, England, United Kingdom

Postcode: RG41 5TS

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Soft-tissue biopsy procedure kit, non-medicated - UK MHRA Medical Device Registration

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