wry QUALITY SY STEM CERTIFICATE concerning medical devices, Annex II, Section 3. Manufacturer: Planmeca Oy Asentajankatu6 FIN-00880 Helsinki Finland coverage of certificate: Design,manufacture and final inspection Productcategory: Dental diagnosti c X-ray equipmentand accessories. Dental units and patient chairs 23rdNovember 2010 Council Directive 93l42lEEC of 14June 1993 Valid until: The manufacturer'squality systemfor the design,manufacture and final inspection of the aforesaid product categoryhas been evaluated and meetsthe provisions of Council Directive 93l42lEEC as setout in Annex II Section 3. This approval is valid until the expiry dateprovided that the manufacturer fulfils the obligations imposed by Annex II in Directive 93l42|EEC. This Certificate is based on decision no. v TT -C -2287 -0 r - | 007 -3 05 -07-P0. SeppoLavonen Certificate no. v TT -C -2287 -0 | - 1 007 -3 05 -07 Translated from Finnish orisinal. Kaarle Kylmiilii Notified Bodv no. 0537: Technical Research Centre of Finland P.O. Box 1300 (Tekniikankatu 1) FIN-33IOI TAMPERE Tel.+358 3 316 3l ll Tampere, 23rdNovember 2007 ffi sl _&,, ffi -M
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coverage of certificate: Design, manufacture and final inspection
Product category: Dental diagnosti c X-ray equipment andaccessories. Dental units and patient chairs
23rd November 2010
Council Directive 93l42lEEC of 14 June 1993
Valid until:
The manufacturer's quality system for the design, manufacture and final inspectionof the aforesaid product category has been evaluated and meets the provisions ofCouncil Directive 93l42lEEC as set out in Annex II Section 3. This approval is validuntil the expiry date provided that the manufacturer fulfils the obligations imposedby Annex II in Directive 93l42|EEC. This Certificate is based on decision no.v TT -C -2287 -0 r - | 007 -3 05 -07-P0.
Seppo Lavonen
Certificate no.
v TT -C -2287 -0 | - 1 007 -3 0 5 -07
Translated from Finnish orisinal.
Kaarle Kylmiilii
Notif ied Bodv no. 0537:Technical Research Centre of FinlandP.O. Box 1300 (Tekniikankatu 1)
FIN-33IOI TAMPERETel .+358 3 316 3 l l l
Tampere, 23rd November 2007
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DE.CISIONon a quality system and product range covered, based on CouncilDirective 93l42lEEC of 14 June 1993 concerning medical devices,
Annex II. Section 3.
Decision no.: vTT -C-2287-0 1 -1 007-305-07-P0Extension of the validity period.
Justification: The manufacturer's certificate no. TUO 1007-206 expires23rdNovember 2007. The manufacturer's quality system has beenreassessed and VTT has found that the quality system and theproducts meet the requirements of Annex II of Medical DeviceDirective 93l42lEEC in design, manufacture and final inspection.The decision is based on the audit report no. NB-I007-A16 andChange Assessment Report No.NB- 1 007-MR08.
VTT is Notified Body no 0537 under Council Directive 93l42lEEC.VTT TEGHNICAL RESEARCH GENTRE OF FINLANDMedical Device TechnologyTekniikankatu 1, Tampere Tel. +358 20 722 111 www.vtt.fiP.O. BOX 1300, Fl-33101 TAMPERE Fax+358 207223365 Business tD0244679-4FINLAND
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The company has signed the undertaking to follow the obligationsof Annex II of the Directive.
vTT -C-2287-0 1 -1007-305-07
Valid until: This decision is valid until23'd November 2010.