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Surgical Kit - ANVISA Registration 81883010010

Access comprehensive regulatory information for Surgical 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 81883010010 and manufactured by TULIP MEDICAL PRODUCTS, INC.. The registration is held by REGEN IMPORT MATERIAIS MÉDICOS E HOSPITALARES LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including MARDEN MEDICAL LTDA, Humanna Medical Ltda, and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.

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81883010010
Registration Details
ANVISA Registration Number: 81883010010
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Device Details

KIT TULIP SOFTBREAST GEMS
Risk Class II

Registration Details

81883010010

25351069825202041

31535015000188

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

May 11, 2020

VIGENTE

09/18/2025 19:00:01