Cavity-wound management dressing, non-antimicrobial - UK MHRA Medical Device Registration

Cavity-wound management dressing, non-antimicrobial is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 88329. The device is manufactured by 3M Company 3M Health Care from United States, classified as General Medical Device. The authorized representative in the UK is 3M United Kingdom PLC.

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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Cavity-wound management dressing, non-antimicrobial

MHRA Device ID: 88329•Ref: 88329

Device Type

General Medical Device

Devices

Cavity-wound management dressing, non-antimicrobial

Type

Class IIb

Date Registered

Apr 11, 2024

Last Updated

Feb 28, 2024

Manufacturer Information

Name

3M Company 3M Health Care

Address

3M Center 2510 Conway Ave

Saint Paul, Minnesota, United States

Created Date

Mar 25, 2021

Authorized Representative

Name

3M United Kingdom PLC

Relationship Type

UK Responsible Person

Address

Cain Road

Bracknell, Berkshire, United Kingdom

Postcode: RG12 8HT

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Other Products from 3M Company 3M Health Care (10)

Other Products from Same Authorized Representative (10)

Cavity-wound management dressing, non-antimicrobial - 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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