Marktintelligenz

Brazil

Medizinprodukt-Marktintelligenz für Brazil. Regulatorische Änderungen, Wettbewerber und Beschaffungstrends.

89
Signals / 7 days
184
Activity Score
ANVISA
ANVISA Registration · GMP Certificate

Neueste Signale

reg_registration2026-05-25

Nutec Global Industria e Comercio Ltda is registered with the FDA under product code FGY.

FDA Device Registration & Listing ·
reg_enforcement2026-05-20

A Phase I/II trial will assess an AI-integrated 3D-printed videolaryngoscope for intubation in critically ill patients.

ClinicalTrials.gov · 2027-03-20
reg_enforcement2026-05-18

AngioSeal device shows non-inferiority in vascular complications versus radial access in acute coronary syndrome patients.

ClinicalTrials.gov · 2012-07-01
reg_enforcement2026-05-14

Endoscopic closure of tracheoesophageal fistulas using a cardiac septal defect occluder device has been terminated.

ClinicalTrials.gov · 2010-06-01
com_launch2026-05-13

A study compares an innovative 3-lead wireless Holter system to a conventional one for cardiac arrhythmia detection.

ClinicalTrials.gov · 2021-01-26
reg_registration2026-05-12

AC Equipamentos Medicos e Odontologicos LTDA has FDA registration 3021741513 for product code KLC.

FDA Device Registration & Listing ·
reg_registration2026-05-12

ARTHREX, INC. has registered a medical device with the FDA under product code HRX.

FDA Device Registration & Listing ·
com_launch2026-05-08

A new device for vestibular evoked myogenic potential shows similar bioelectrical responses to the gold standard device.

ClinicalTrials.gov ·
reg_enforcement2026-05-07

The Canabrava Ring was evaluated for safety and efficacy in cataract surgery on small pupils in a completed study.

ClinicalTrials.gov · 2014-09-01
reg_registration2026-05-06

The L6R T-ONE SP NC ROTH .022 device by ID-LOGICAL is classified as Class IIa and registered in EUDAMED.

EUDAMED EU Device Database ·
com_launch2026-05-05

A study tested the DUDA Device to prevent cervical stenosis after conization in high-grade cervical dysplasia.

ClinicalTrials.gov · 2015-08-01
reg_registration2026-05-05

TOYO COMERCIO has registered a surgical instruments firm with FDA under product code HTE.

FDA Device Registration & Listing ·
reg_registration2026-05-05

Ortho Pauher has registered a medical device with the FDA under product code KNO.

FDA Device Registration & Listing ·
reg_registration2026-05-05

Indusbello Ind. e Com. de Prod. Med. e Odont. Ltda. registered a medical device with product code KCQ.

FDA Device Registration & Listing ·
com_launch2026-05-04

Study completed on using Occlutech Figulla ASD N for bronchopleural fistula closure via bronchoscopy.

ClinicalTrials.gov · 2010-06-01
reg_registration2026-05-01

Aditek do Brasil SA registered the KIT 5X5 EASYCLIP+ PASSIVE 018 MBT HK 3 W/20 as a Class IIA medical device.

EUDAMED EU Device Database ·
reg_registration2026-05-01

Aditek do Brasil SA registered the KIT 5X5 EASYCLIP+ PASSIVE 018 MBT HK 3,4,5 W/20 as Class IIA device.

EUDAMED EU Device Database ·
reg_registration2026-05-01

Aditek do Brasil SA registered the BRACKET EASYCLIP+ PASSIVE 018, classified as Class IIa medical device.

EUDAMED EU Device Database ·
reg_registration2026-05-01

Aditek do Brasil SA registered the BRACKETEASYCLIP+ PASSIVE 018 device as Class IIA in EUDAMED.

EUDAMED EU Device Database ·
reg_enforcement2026-04-28

A study is assessing a heart monitor's effectiveness post-myocardial infarction in patients over 18 years.

ClinicalTrials.gov · 2019-05-01

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