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ANCHOR - ANVISA Registration 80120790084

Access comprehensive regulatory information for ANCHOR in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80120790084 and manufactured by Parcus Medical L.L.C. The registration is held by OPTIKA SISTEMAS PARA MEDICINA S/A with validity until Jul 22, 2029.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including STRYKER ENDOSCOPY, SMITH & NEPHEW INC., ENDOSCOPY DIVISION (ANDOVER), 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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80120790084
2 Related Devices
Registration Details
ANVISA Registration Number: 80120790084
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Related Devices (2)

ร‚ncora de sutura PEEK CF Push-In sem nรณ
Risk Class III

Registration Details

80120790084

25351730009201827

04579646000126

Company Information

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

Dates and Status

Jul 22, 2019

22/07/2029

09/18/2025 19:00:01

ร‚ncora de sutura PEEK CF Push-In sem nรณ
Risk Class III

Registration Details

80120790084

25351730009201827

04579646000126

Company Information

Dates and Status

Jul 22, 2019

22/07/2029

09/18/2025 19:00:01