PHENOBARBITAL* - ANVISA Registration 80254180458
Access comprehensive regulatory information for PHENOBARBITAL* in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80254180458 and manufactured by MICROGENICS CORPORATION. The registration is held by PHADIA DIAGNOSTICOS LTDA with validity until Jun 26, 2033.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search. 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.

Janaina dos Santos de Miranda
🇧🇷 Brazil Regulatory Expert
Need help with your Brazil registration?
Contact Pure Global Brazil TeamRelated Devices (2)
Registration Details
80254180458
25351152783202351
04930429000139
Company Information
Dates and Status
Jun 26, 2023
26/06/2033
09/18/2025 19:00:01
PHENYTOIN
CEDIA Phenytoin II Assay
Not specified
80254180459
Jul 03, 2023
PHENYTOIN
CEDIA Phenytoin II Assay
MICROGENICS CORPORATION
80254180459
Jul 03, 2023
PHENOBARBITAL
ADVIA CENTAUR PHNB
SIEMENS HEALTHCARE DIAGNOSTICS INC
10345160389
Jun 23, 2003
PHENOBARBITAL
Atellica CH Fenobarbital (Phnb)
SIEMENS HEALTHCARE DIAGNOSTICS INC.
10345162136
Dec 04, 2017
CARBAMAZEPINE
CEDIA Carbamazepine II Assay
Not specified
80254180388
May 31, 2021