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ANVISA registration 80822699001Active

Ultrasound-guided peripheral nerve block cannula

ANVISA Registration Number: 80822699001ATCS COMERCIO E SERVICOS DE EQUIPAMENTOS MEDICOS LTDA - EPPPAJUNK GMBH MEDIZINTECHNOLOGIERisk Class II
Verified
Device names
Technical name
Ultrasound-guided peripheral nerve block cannula
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PT: Cânula de bloqueio de nervos periféricos por ultrassom
Commercial name
HYBRID PAIN SYSTEM
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Risk class
Class II
Registration details
Registration Number
80822699001
Process Number
25351239792202275
CNPJ
01028682000103
Company information
Registration Holder
ATCS COMERCIO E SERVICOS DE EQUIPAMENTOS MEDICOS LTDA - EPP
Manufacturer
PAJUNK GMBH MEDIZINTECHNOLOGIE
Manufacturing Country
Germany
PT: ALEMANHA
Dates and status
Publication Date
Apr 07, 2022
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Ultrasound-guided peripheral nerve block cannula in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80822699001 and manufactured by PAJUNK GMBH MEDIZINTECHNOLOGIE. The registration is held by ATCS COMERCIO E SERVICOS DE EQUIPAMENTOS MEDICOS LTDA - EPP with validity until currently active (VIGENTE).

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.