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Components for External Orthotics and Prosthetics - ANVISA Registration 10356020109

Access comprehensive regulatory information for Components for External Orthotics and Prosthetics in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10356020109 and manufactured by DREVE-OTOPLASTIK GMBH. The registration is held by CENTRO AUDITIVO TELEX 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 ÖSSUR HEAD OFFICE, OTTOBOCK SE & CO KGAA, 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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10356020109
Registration Details
ANVISA Registration Number: 10356020109
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Device Details

OTOFORM Material de impressão à base de silicone
Risk Class I

Registration Details

10356020109

25351144778201707

33060302000104

Company Information

Germany
PT: ALEMANHA

Dates and Status

Apr 17, 2017

VIGENTE

09/18/2025 19:00:01