Surgical/emergency suction cannula, non-illuminating, single-use - UK MHRA Medical Device Registration

Surgical/emergency suction cannula, non-illuminating, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 120450. The device is manufactured by Mediplast AB from Sweden, classified as General Medical Device. The authorized representative in the UK is Qserve Group 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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Surgical/emergency suction cannula, non-illuminating, single-use

MHRA Device ID: 120450•Ref: 120450

Device Type

General Medical Device

Devices

Surgical/emergency suction cannula, non-illuminating, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Name

Mediplast AB

Address

Bronsåldersgatan 2

Malmö, Sweden

Created Date

Dec 13, 2021

Authorized Representative

Name

Qserve Group UK, Ltd.

Relationship Type

UK Responsible Person

Address

49 Greek Street

London, England, United Kingdom

Postcode: W1D 4EG

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Other Products from Mediplast AB (10)

Other Products from Same Authorized Representative (10)

Surgical/emergency suction cannula, non-illuminating, 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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