Lancets - ANVISA Registration 10270099001
Access comprehensive regulatory information for Lancets in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10270099001 and manufactured by LINCOLN DIAGNOSTICS, INC. The registration is held by VITAFARMA IMPORTAÇÃO E DISTRIBUIDORA DE SUPLEMENTOS ALIMENTARES LTDA with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including SteriLance Medical (SuZhou) Inc., TIANJIN HUAHONG TECHNOLOGY CO., LTD., 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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Registration Details
10270099001
25351322031201019
85054096000123
Company Information
Dates and Status
Jan 02, 2012
VIGENTE
09/18/2025 19:00:01
Lancets
DUOTIP - TEST® II
LINCOLN DIAGNOSTICS, INC
10270090003
Apr 01, 2013
Lancets
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SteriLance Medical (SuZhou) Inc.
81596329001
Mar 26, 2018
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Multi-Test® PC
LINCOLN DIAGNOSTICS, INC
81900289001
Dec 17, 2020
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DuoTip-Test® II
LINCOLN DIAGNOSTICS, INC
81900289002
Dec 23, 2020
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AUTO LANCETA II BIOLAND
SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD
10410130025
Nov 23, 2015
SteriLance Medical (SuZhou) Inc.• China
TIANJIN HUAHONG TECHNOLOGY CO., LTD.• China
STERILANCE MEDICAL (SUZHOU) INC.• China
SUZHOU KYUAN MEDICAL APPARATUS CO., LTD.• China
TIANJIN RILIFINE MEDICAL DEVICE CO., LTD.• China
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