ANVISA registration 80444810030Valid until Nov 28, 2026Posterior spinal system for fixation in lamina, pedicle, apophysis or articular mass.
ANVISA Registration Number: 80444810030HIGHRIDGE MEDICAL BRASIL LTDALDR MEDICALRisk Class III
Device names
- Technical name
- Posterior spinal system for fixation in lamina, pedicle, apophysis or articular mass.
- Commercial name
- InterBRIDGE® Sistema de fixação posterior interespinhoso
- Risk class
- Class III
PT: Sistema posterior de coluna para fixação em lâmina, pedículo, apófise ou maciço articular.
Registration details
- Registration Number
- 80444810030
- Process Number
- 25351589538201582
- CNPJ
- 08954683000128
Company information
- Registration Holder
- HIGHRIDGE MEDICAL BRASIL LTDA
- Manufacturer
- LDR MEDICAL
- Manufacturing Country
- France
PT: FRANÇA
Dates and status
- Publication Date
- Nov 28, 2016
- Validity
- 28/11/2026
- 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 80444810030 and manufactured by LDR MEDICAL. The registration is held by HIGHRIDGE MEDICAL BRASIL LTDA with validity until Nov 28, 2026.
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