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 - Pierrel Pharma S.r.l

Address:

Strada Statale Appia 7 bis 46-48

Capua

81043

Italy

Authorised Representative/ UK Responsible Person
Name: DENTAL SKY WHOLESALER LTD
Address:

Unit A Foster Road Ashford Business Park Sevington

ASHFORD

ASHFORD

Kent TN24 0SH

England United Kingdom

Code/Term Type

Body fluorescence scanning system Body fluorescence scanning system Class I

Needle recapping device reusable Needle recapping device reusable Class I

Periodontal tissue reconstructive material Periodontal tissue reconstructive material Class IIa

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
Body fluorescence scanning system	Body fluorescence scanning system	Class I
Needle recapping device reusable	Needle recapping device reusable	Class I
Periodontal tissue reconstructive material	Periodontal tissue reconstructive material	Class IIa