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Surgical Sponge - ANVISA Registration 80320689020

Access comprehensive regulatory information for Surgical Sponge in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80320689020 and manufactured by HEMOSTASIS LLC. The registration is held by DANIALEX TEC - MATERIAL MEDICO HOSPITALAR LTDA ME 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 G. SURGIWEAR LIMITED, Tecfen Medical, 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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80320689020
Registration Details
ANVISA Registration Number: 80320689020
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Device Details

Vectra F
Risk Class II

Registration Details

80320689020

25351070124202560

01686305000161

Company Information

HEMOSTASIS LLC
United States of America
PT: ESTADOS UNIDOS DA AMร‰RICA

Dates and Status

May 12, 2025

VIGENTE

09/18/2025 19:00:01