Cranial orthosis - UK MHRA Medical Device Registration

Cranial orthosis is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 122842. The device is manufactured by e-life International Co., Ltd. from Taiwan, classified as General Medical Device. The authorized representative in the UK is MDSS-UK RP LIMITED.

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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Cranial orthosis

MHRA Device ID: 122842•Ref: 122842

Device Type

General Medical Device

Devices

Cranial orthosis

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Oct 16, 2024

Manufacturer Information

Name

e-life International Co., Ltd.

Address

7F, No. 1, Baosheng Rd., Yonghe Dist.

New Taipei City, Taiwan

Created Date

Dec 17, 2021

Authorized Representative

Name

MDSS-UK RP LIMITED

Relationship Type

UK Responsible Person

Address

6 Wilmslow Road, Rusholme

Manchester, England, United Kingdom

Postcode: M14 5TP

DJ Fang

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Other Products from e-life International Co., Ltd. (10)

Other Products from Same Authorized Representative (10)

Cranial orthosis - 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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