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Forceps - ANVISA Registration 80145901155

Access comprehensive regulatory information for Forceps in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80145901155 and manufactured by CODMAN & SHURTLEFF INC.. The registration is held by JOHNSON & JOHNSON DO BRASIL INDÚSTRIA E COMÉRCIO DE PRODUTOS PARA SAÚDE LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for 3 related devices, regulatory compliance details, 5 companies making the same product including KOLPLAST CI LTDA, WEXLER SURGICAL SUPPLIES, 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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80145901155
3 Related Devices
Registration Details
ANVISA Registration Number: 80145901155
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Related Devices (3)

INSTRUMENTAL CIRÚRGICO CODMAN PINÇAS NÃO ARTICULADAS DE TITÂNIO
Risk Class I

Registration Details

80145901155

25351059146200878

54516661000101

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Sep 22, 2008

VIGENTE

09/18/2025 19:00:01

INSTRUMENTAL CIRÚRGICO CODMAN PINÇAS NÃO ARTICULADAS DE TITÂNIO
Risk Class I

Registration Details

80145901155

25351059146200878

54516661000101

Company Information

ETHICON GMBH
Germany
PT: ALEMANHA

Dates and Status

Sep 22, 2008

VIGENTE

09/18/2025 19:00:01

INSTRUMENTAL CIRÚRGICO CODMAN PINÇAS NÃO ARTICULADAS DE TITÂNIO
Risk Class I

Registration Details

80145901155

25351059146200878

54516661000101

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Sep 22, 2008

VIGENTE

09/18/2025 19:00:01