ANVISA registration 80102512803Valid until May 02, 2032SPINAL FUSION CAGES
ANVISA Registration Number: 80102512803VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDAMEDACTA INTERNATIONAL S.A.Risk Class III
Device names
- Commercial name
- DISPOSITIVO DE FUSÃO TRANSFORAMINAL MECTALIF TiPEEK
- Risk class
- Class III
Registration details
- Registration Number
- 80102512803
- Process Number
- 25351716874202166
- CNPJ
- 04718143000194
Company information
- Registration Holder
- VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA
- Manufacturer
- MEDACTA INTERNATIONAL S.A.
- Manufacturing Country
- Switzerland
PT: SUÍÇA
Dates and status
- Publication Date
- May 02, 2022
- Validity
- 02/05/2032
- Last Updated
- 08/18/2026 19:00:00
About this record
Access comprehensive regulatory information for SPINAL FUSION CAGES in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80102512803 and manufactured by MEDACTA INTERNATIONAL S.A.. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until May 02, 2032.
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