ANVISA registration 10355870315Active

SINGLE USE VACUUM TUBE

Name: SINGLE USE VACUUM TUBE — ANVISA registration 10355870315
Creator: Katalyst Surgical, LLC
Keywords: SINGLE USE VACUUM TUBE, TUBO PARA VACUO, DE USO UNICO, Tubos Kogent, 10355870315, Risk Class II, ANVISA registration

ANVISA Registration Number: 10355870315BIOMÉDICA EQUIPAMENTOS E SUPRIMENTOS HOSPITALARES LTDAKatalyst Surgical, LLCRisk Class II

Verified

Device names

Technical name: SINGLE USE VACUUM TUBE
Commercial name: Tubos Kogent
Risk class: Class II

Registration details

Registration Number: 10355870315
Process Number: 25351484171201787
CNPJ: 01299509000140

Company information

Registration Holder: BIOMÉDICA EQUIPAMENTOS E SUPRIMENTOS HOSPITALARES LTDA
Manufacturer: Katalyst Surgical, LLC
Manufacturing Country: United States

Dates and status

Publication Date: Dec 18, 2017
Validity: VIGENTE
Last Updated: 08/18/2026 19:00:00

About this record

Access comprehensive regulatory information for SINGLE USE VACUUM TUBE in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10355870315 and manufactured by Katalyst Surgical, LLC. The registration is held by BIOMÉDICA EQUIPAMENTOS E SUPRIMENTOS HOSPITALARES LTDA with validity until currently active (VIGENTE).

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