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Suture Kit - ANVISA Registration 81464750165

Access comprehensive regulatory information for Suture Kit in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81464750165 and manufactured by manufacturer not specified. The registration is held by Domo Salute Consultoria Regulatória Ltda with validity until Oct 29, 2034.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including VIVA CARE MATERIAL MEDICO HOSPITALAR LTDA, KOLPLAST CI 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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81464750165
2 Related Devices
Registration Details
ANVISA Registration Number: 81464750165
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Related Devices (2)

BIOTEK Dispositivo de reparação de Menisco (All inside)
Risk Class III

Registration Details

81464750165

25351679023202397

26263959000103

Company Information

Dates and Status

Oct 29, 2024

29/10/2034

09/18/2025 19:00:01

BIOTEK Dispositivo de reparação de Menisco (All inside)
Risk Class III

Registration Details

81464750165

25351679023202397

26263959000103

Company Information

India
PT: ÍNDIA

Dates and Status

Oct 29, 2024

29/10/2034

09/18/2025 19:00:01