Peripheral artery cannula - UK MHRA Medical Device Registration

Peripheral artery cannula is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 88433. The device is manufactured by Delta Med SpA from Italy, classified as General Medical Device. The authorized representative in the UK is Donawa Lifescience Ltd.

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Peripheral artery cannula

MHRA Device ID: 88433•Ref: 88433

Device Type

General Medical Device

Devices

Peripheral artery cannula

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Apr 13, 2024

Manufacturer Information

Name

Delta Med SpA

Address

Via G. Rossa 20

Viadana, Mantova, Italy

Created Date

Jul 5, 2021

Authorized Representative

Name

Donawa Lifescience Ltd

Relationship Type

UK Responsible Person

Address

Aviation Business Park Enterprise Close

Christchurch, England, United Kingdom

Postcode: BH23 6NX

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Other Products from Delta Med SpA (10)

Other Products from Same Authorized Representative (10)

Peripheral artery cannula - 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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