General-purpose medical foam padding, reusable - UK MHRA Medical Device Registration

General-purpose medical foam padding, reusable is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 203975. The device is manufactured by Biodermis LLC from United States, classified as General Medical Device. The authorized representative in the UK is MDSS-UK RP 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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General-purpose medical foam padding, reusable

MHRA Device ID: 203975•Ref: 203975

Device Type

General Medical Device

Devices

General-purpose medical foam padding, reusable

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Oct 30, 2024

Manufacturer Information

Name

Biodermis LLC

Address

1820 Whitney Mesa Dr, Suite 100

Henderson, NV, United States

Created Date

Oct 25, 2024

Authorized Representative

Name

MDSS-UK RP LIMITED

Relationship Type

UK Responsible Person

Address

6 Wilmslow Road, Rusholme

Manchester, England, United Kingdom

Postcode: M14 5TP

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Other Products from Biodermis LLC (2)

Scar-management dressing, single-use

Type: General Medical Device

Registered: Nov 26, 2024

Scar-management dressing, reusable

Type: General Medical Device

Registered: Nov 26, 2024

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General-purpose medical foam padding, reusable - UK MHRA Medical Device Registration

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