ANVISA registration

Kit Ionolux Application Capsules

Registration 80230400076. Ionomero de Vidro Modificado por Resina

Registration details

Registration number80230400076
Application number25351712347201968
Technical nameIonomero de Vidro Modificado por Resina
Risk classII
Published on27/01/2020
ValidityIndefinite validity

Registration holder

Legal nameVOCO DO BRASIL LTDA
CNPJ05.915.452/0001-17

Manufacturer

  • VOCO GMBH ALEMANHA

Other registrations held by VOCO DO BRASIL LTDAview all

UFI GEL SC UFI GEL P

80230400002

POLOFIL SUPRA

80230400007

FISSURIT F / FISSURIT FX

80230400008

BIFLUORID 12

80230400009

GRANDIO

80230400010

ADMIRA

80230400011

Source: ANVISA

Source: ANVISA open data, medical device file, updated daily. The public database provides registration validity, rather than registration status: this registration may have been cancelled before its expiry date without this being shown here. Before making purchasing, import or marketing decisions, check the ANVISA search portal.

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