Medical Device & Regulatory Information
Supply of Tulip Medical Products in Great Britain.
Last updated: 20 June 2026
Professional Use Only
Products are medical devices for qualified healthcare professionals only.
UK Regulatory Framework
Devices must comply with the Medical Devices Regulations 2002 (SI 2002/618, as amended), enforced by the MHRA.
MHRA Registration
All devices must be MHRA-registered by the manufacturer or UK Responsible Person before GB market placement.
CE & UKCA Marking
Under current MHRA transitional arrangements, CE-marked devices continue to be accepted. Refer to product IFU for marking details.
Simyamed Medical as Distributor
- Verify CE/UKCA marking before supply
- Comply with storage and transport requirements
- Maintain distribution records for traceability
- Report adverse incidents to manufacturer and MHRA
Adverse Incident Reporting
- Simyamed Medical: info@simyamedical.co.uk
- MHRA Yellow Card
Geographic Scope
We supply England, Wales and Scotland (Great Britain). For other regions contact Tulip Medical.