Public Access Database for Medical Device Registration

Registration does not represent any form of accreditation, certification or approval by the UK Competent Authority(MHRA)
Where a conformity assessment certificate is listed as expired, existing products already placed on the market prior to the expiry may not be affected by this expiry and can continue to be used. This expiry stops new products being placed on the market until there is a new certificate of conformity

Manufacturer's By Name

By Device

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Manufacturer's Devices - Takeda Pharmaceuticals U.S.A. Inc.

Address:

95 Hayden Ave

Lexington

MA 02421

United States

Authorised Representative/ UK Responsible Person
Name: MT Promedt Consulting Ltd
Address:

Beaver House 23-38 Hythe Bridge Street

Oxford

OX1 2EP

England United Kingdom

Code/Term Type

General-purpose syringe single-use General-purpose syringe single-use

Cartridge-accepting autoinjector mechanical Cartridge-accepting autoinjector mechanical Class I

Cartridge-accepting autoinjector mechanical Cartridge-accepting autoinjector mechanical Class I

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

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Code/Term		Type
General-purpose syringe single-use	General-purpose syringe single-use
Cartridge-accepting autoinjector mechanical	Cartridge-accepting autoinjector mechanical	Class I
Cartridge-accepting autoinjector mechanical	Cartridge-accepting autoinjector mechanical	Class I