Intracranial/spinal endoscope
ANVISA Registration Number: 81901539033DEUTSCHLINE MEDICAL LTDADEUTSCHLINE MEDIZINPRODUKTE GMBHRisk Class II
Device names
- Technical name
- Intracranial/spinal endoscope
- Risk class
- Class II
PT: Endoscópio intracraniano/espinhal
Registration details
- Registration Number
- 81901539033
- Process Number
- 25351199143202577
- CNPJ
- 29763498000126
Company information
- Registration Holder
- DEUTSCHLINE MEDICAL LTDA
- Manufacturer
- DEUTSCHLINE MEDIZINPRODUKTE GMBH
- Manufacturing Country
- Germany
PT: ALEMANHA
Dates and status
- Publication Date
- Dec 08, 2025
- Validity
- VIGENTE
- Last Updated
- 08/18/2026 19:00:00
About this record
Access comprehensive regulatory information for Intracranial/spinal endoscope in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81901539033 and manufactured by DEUTSCHLINE MEDIZINPRODUKTE GMBH. The registration is held by DEUTSCHLINE MEDICAL LTDA with validity until currently active (VIGENTE).
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