Pure Global AI
ANVISA registration 81365089008Active

Instrument Kit

ANVISA Registration Number: 81365089008vertek consumo clinico e hospitalar Ltda meMEDICAL INSTRUMENT DEVELOPMENT LABORATORIES (MIDLABS INC.)Risk Class II
Verified
Device names
Technical name
Instrument Kit
View exact technical-name matches →
PT: Kit Instrumental
Commercial name
CÂNULA DE INSERÇÃO
View exact commercial-name matches →
Risk class
Class II
Registration details
Registration Number
81365089008
Process Number
25351149912202596
CNPJ
22898875000195
Company information
Registration Holder
vertek consumo clinico e hospitalar Ltda me
Manufacturer
MEDICAL INSTRUMENT DEVELOPMENT LABORATORIES (MIDLABS INC.)
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Sep 08, 2025
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Instrument Kit in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81365089008 and manufactured by MEDICAL INSTRUMENT DEVELOPMENT LABORATORIES (MIDLABS INC.). The registration is held by vertek consumo clinico e hospitalar Ltda me 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.