Manual scalpel blade, single-use - UK MHRA Medical Device Registration

Manual scalpel blade, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 179385. The device is manufactured by Surgistar Inc from United States, classified as General Medical Device. The authorized representative in the UK is Wellkang 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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Manual scalpel blade, single-use

MHRA Device ID: 179385•Ref: 179385

Device Type

General Medical Device

Devices

Manual scalpel blade, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Sep 30, 2024

Manufacturer Information

Name

Surgistar Inc

Address

Surgistar Inc La Mirada Dr 2310

Vista, United States

Created Date

Sep 22, 2023

Authorized Representative

Name

Wellkang Ltd

Relationship Type

Authorised Representative (Northern Ireland)

Address

Enterprise Hub, NW Business Complex 1 Beraghmore Road

Derry, Northern Ireland, Northern Ireland, United Kingdom

Postcode: BT48 8SE

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Manual scalpel blade, single-use - UK MHRA Medical Device Registration

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Date Registered

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Created Date

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