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 - NEOFECT Co. Ltd.

Address:

#801 42

Changeop-Ro Sujeong-Gu

Gyeonggi-Do

Seongnam-Si 13449

South Korea

Authorised Representative/ UK Responsible Person
Name: Baffin Technology Systems Ltd
Address:

Bragborough Hall Business Centre Welton Road

Braunston

NN11 7JG

England United Kingdom

Code/Term Type

Virtual-display rehabilitation system non-supportive clinical Virtual-display rehabilitation system non-supportive clinical Class I

Elbow/wrist/hand orthosis Elbow/wrist/hand orthosis Class I

Hand orthosis Hand orthosis Class I

Ankle/foot orthosis Ankle/foot orthosis 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
Virtual-display rehabilitation system non-supportive clinical	Virtual-display rehabilitation system non-supportive clinical	Class I
Elbow/wrist/hand orthosis	Elbow/wrist/hand orthosis	Class I
Hand orthosis	Hand orthosis	Class I
Ankle/foot orthosis	Ankle/foot orthosis	Class I