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

Back to MHRA

Manufacturer's Devices - Adroit Surgical LLC

Address:

10001 Broadway Extension Suite A

Oklahoma City

73114

United States

Authorised Representative/ UK Responsible Person
Name: Obelis UK Ltd
Address:

Sandford Gate East Point Business Park

Oxford

OX4 6LB

England United Kingdom

Code/Term Type

Oesophageal bougie single-use Oesophageal bougie single-use Class I

Rigid intubation laryngoscope single-use Rigid intubation laryngoscope single-use Class I

Endotracheal tube introducer single-use Endotracheal tube introducer single-use Class I

Contact details

Freedom of information

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

© 2011 Crown Copyright. To contact us about this website, use our feedback form.

Code/Term		Type
Oesophageal bougie single-use	Oesophageal bougie single-use	Class I
Rigid intubation laryngoscope single-use	Rigid intubation laryngoscope single-use	Class I
Endotracheal tube introducer single-use	Endotracheal tube introducer single-use	Class I