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ANVISA registration 10383709004Active

Ultrasound-guided peripheral nerve block cannula

ANVISA Registration Number: 10383709004VK DRILLER EQUIPAMENTOS ELÉTRICOS LTDAVK DRILLER EQUIPAMENTOS ELÉTRICOS LTDARisk 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
KIT DE CÂNULA GOLDEN BLOCK
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Risk class
Class II
Registration details
Registration Number
10383709004
Process Number
25351520441202115
CNPJ
68996560000181
Company information
Registration Holder
VK DRILLER EQUIPAMENTOS ELÉTRICOS LTDA
Manufacturer
VK DRILLER EQUIPAMENTOS ELÉTRICOS LTDA
Manufacturing Country
Brazil
PT: BRASIL
Dates and status
Publication Date
Jun 02, 2021
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 10383709004 and manufactured by VK DRILLER EQUIPAMENTOS ELÉTRICOS LTDA. The registration is held by VK DRILLER EQUIPAMENTOS ELÉTRICOS LTDA 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.