ANVISA registration 80102513141Valid until May 02, 2027Posterior spinal system for fixation in lamina, pedicle, apophysis or articular mass.
ANVISA Registration Number: 80102513141VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDAULRICH GMBH & CO.KG.Risk Class III
Device names
- Technical name
- Posterior spinal system for fixation in lamina, pedicle, apophysis or articular mass.
- Risk class
- Class III
PT: Sistema posterior de coluna para fixação em lâmina, pedículo, apófise ou maciço articular.
Registration details
- Registration Number
- 80102513141
- Process Number
- 25351772453202387
- CNPJ
- 04718143000194
Company information
- Registration Holder
- VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA
- Manufacturer
- ULRICH GMBH & CO.KG.
- Manufacturing Country
- Germany
PT: ALEMANHA
Dates and status
- Publication Date
- Dec 04, 2023
- Validity
- 02/05/2027
- Last Updated
- 08/18/2026 19:00:00
About this record
Access comprehensive regulatory information for Posterior spinal system for fixation in lamina, pedicle, apophysis or articular mass. in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80102513141 and manufactured by ULRICH GMBH & CO.KG.. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until May 02, 2027.
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