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Medical device registration with ANVISA
Search by number, product, registration holder or CNPJ. The data comes from ANVISA's open data publications and is updated here daily.
Registrations held by TELEFLEX MEDICAL BRASIL LTDAremove
80 registrations
| Product | Registration holder | Class | Validity |
|---|---|---|---|
| Tubo Endotraqueal Oral/Nasal Magill sem balão80312279042 | TELEFLEX MEDICAL BRASIL LTDA | II | Valid |
| Tubos Endobrônquicos SHERIDAN SHER-I-BRONCH®80312279039 | TELEFLEX MEDICAL BRASIL LTDA | II | Valid |
| Vias Aéreas Orofaríngeas CATH-GUIDE®80312279046 | TELEFLEX MEDICAL BRASIL LTDA | II | Valid |
| Válvula PEEP80312279065 | TELEFLEX MEDICAL BRASIL LTDA | II | Valid |
| Weck EFx Shield Fascial Closure System80312279053 | TELEFLEX MEDICAL BRASIL LTDA | II | Valid |
Source: ANVISA open data, medical device file. The database provides registration validity, rather than registration status: a registration may have been cancelled before its expiry date without this being shown here. Before making purchasing, import or marketing decisions, check the ANVISA search portal.
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HSC manages medical device registration with ANVISA, from risk classification to monitoring the application.
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