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Lancet - ANVISA Registration 80695719035

Access comprehensive regulatory information for Lancet in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80695719035 and manufactured by HTL STREFA S.A. The registration is held by BIOTEC BIOLOGICA INDÚSTRIA FARMACÊUTICA 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 TIANJIN HUAHONG TECHNOLOGY CO., LTD., STERILANCE MEDICAL (SUZHOU) INC., 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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80695719035
Registration Details
ANVISA Registration Number: 80695719035
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Device Details

Acti-Lance
Risk Class II

Registration Details

80695719035

25351850658202319

10446719000104

Company Information

HTL STREFA S.A
Poland
PT: POLÔNIA

Dates and Status

Apr 15, 2024

VIGENTE

09/18/2025 19:00:01