Filiform urethral bougie - UK MHRA Medical Device Registration

Filiform urethral bougie is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 134520. The device is manufactured by STEMA Medizintechnik GmbH from Germany, classified as General Medical Device. The authorized representative in the UK is Compliance Solutions (Lifesciences) 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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Filiform urethral bougie

MHRA Device ID: 134520•Ref: 134520

Device Type

General Medical Device

Devices

Filiform urethral bougie

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Apr 23, 2024

Manufacturer Information

Name

STEMA Medizintechnik GmbH

Address

take-off GewerbePark 74

Neuhausen ob Eck, Germany

Created Date

Jul 14, 2021

Authorized Representative

Name

Compliance Solutions (Lifesciences) Ltd

Relationship Type

UK Responsible Person

Address

Suite 10, Dunswood House 1 Dunswood Road Cumbernauld

Glasgow, United Kingdom

Postcode: G67 3EN

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Filiform urethral bougie - UK MHRA Medical Device Registration

Device Type

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Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

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