OPTILASA S.L. - BEUDAMED

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1 results · 27ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 2 ×

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Classification

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FDA FEI Number

1000159913 1 1000175127 1 1000181430 1 1000391004 1 1000582291 1 1926681 1 2521877 1 2936921 1 3001362763 1 3002398337 1 3002439654 1 3002680900 1 3002785343 1 3002807715 1 3002807782 1 3002808293 1 3002809378 1 3003617485 1 3003768492 1 3003771740 1 + More FDA FEI Numbers

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FDA Registration Number

1000181430 1 1000391004 1 1319721 1 1926681 1 2521877 1 2936921 1 3002439654 1 3002807715 1 3003617485 1 3003771740 1 3004026651 1 3004443844 1 3004681519 1 3004848970 1 3005301392 1 3005324856 1 3005771344 1 3007075140 1 3008396732 1 3008559295 1 + More FDA Registration Numbers

APPLANATION TONOMETER

FDA Class 2 ·Ophthalmic

Data last updated 04 / 2026. Visit the official EUDAMED website for up-to-date data.

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EU IVDR

EU IVDR In Vitro Diagnostic Devices EU IVDR Class A In Vitro Diagnostic Devices EU IVDR Class A Software Devices EU IVDR Class B In Vitro Diagnostic Devices EU IVDR Class B Software Devices EU IVDR Class C In Vitro Diagnostic Devices EU IVDR Class C Software Devices EU IVDR Class D In Vitro Diagnostic Devices EU IVDR Class D Software Devices EU IVDR Instrument Devices EU IVDR Kit Devices EU IVDR Reagent Devices EU IVDR Software Devices

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Notified Bodies

BSI Group The Netherlands B.V. DEKRA Certification B.V. DNV Product Assurance AS POLSKIE CENTRUM BADAN I CERTYFIKACJI S.A. SGS Belgium NV TÜV Rheinland LGA Products GmbH TÜV SÜD Product Service GmbH UDEM Uluslararasi Belgelendirme Denetim Egitim Merkezi San. ve Tic. A.Ş.

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