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ANVISA registration 80208360058Active

Dispositivo Para Fixacao de Cateter

ANVISA Registration Number: 80208360058HEMOCAT COMERCIO E IMPORTACAO LTDATIDI® Products, LLCRisk Class I
Verified
Device names
Technical name
Dispositivo Para Fixacao de Cateter
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Commercial name
Kit de Fixação de Cateter Universal Periférico e Cateter arterial de segurança – GRIP-LOK
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Risk class
Class I
Registration details
Registration Number
80208360058
Process Number
25351223307201713
CNPJ
02993016000178
Company information
Registration Holder
HEMOCAT COMERCIO E IMPORTACAO LTDA
Manufacturer
TIDI® Products, LLC
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
May 29, 2017
Status
Active
Official value: VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Dispositivo Para Fixacao de Cateter in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80208360058 and manufactured by TIDI® Products, LLC. The registration is held by HEMOCAT COMERCIO E IMPORTACAO 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.