Non-woven gauze pad - UK MHRA Medical Device Registration

Non-woven gauze pad is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 172206. The device is manufactured by Orkla 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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Non-woven gauze pad

MHRA Device ID: 172206•Ref: 172206

Device Type

General Medical Device

Devices

Non-woven gauze pad

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Jul 2, 2024

Manufacturer Information

Name

Orkla Care AB

Address

Svetsarvägen 15

Solna, Sweden

Created Date

Aug 27, 2021

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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Non-woven gauze pad - UK MHRA Medical Device Registration

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Date Registered

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Created Date

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