Pressure bandage, non-latex, single-use - UK MHRA Medical Device Registration

Pressure bandage, non-latex, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 172212. The device is manufactured by Orkla Wound Care AB from Sweden, classified as General Medical Device. The authorized representative in the UK is QAdvis 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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Pressure bandage, non-latex, single-use

MHRA Device ID: 172212•Ref: 172212

Device Type

General Medical Device

Devices

Pressure bandage, non-latex, single-use

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Feb 20, 2024

Manufacturer Information

Name

Orkla Wound Care AB

Address

Svetsarvägen 15

Solna, Sweden

Created Date

May 16, 2023

Authorized Representative

Name

QAdvis UK Ltd

Relationship Type

UK Responsible Person

Address

55-66 Frederick Street

Edinburgh, EH2 1LS, Scotland, United Kingdom

Postcode: EH2 1LS

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Other Products from Orkla Wound Care AB (10)

Other Products from Same Authorized Representative (10)

Pressure bandage, non-latex, single-use - 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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