Endomyocardial biopsy forceps, single-use - UK MHRA Medical Device Registration

Endomyocardial biopsy forceps, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 110796. The device is manufactured by Scholten Surgical Instruments, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is Emergo Consulting (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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Endomyocardial biopsy forceps, single-use

MHRA Device ID: 110796•Ref: 110796

Device Type

General Medical Device

Devices

Endomyocardial biopsy forceps, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Oct 15, 2024

Manufacturer Information

Name

Scholten Surgical Instruments, Inc.

Address

170 Commerce Street, Suite 101

Lodi, California, United States

Created Date

Nov 4, 2021

Authorized Representative

Name

Emergo Consulting (UK) Limited

Relationship Type

UK Responsible Person

Address

Compass House, Vision Park Histon c/o Cr360 – UL International

Cambridge, England, United Kingdom

Postcode: CB24 9BZ

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Endomyocardial biopsy forceps, single-use - UK MHRA Medical Device Registration

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