SPINAL FUSION CAGES - ANVISA Registration 80102513139

Access comprehensive regulatory information for SPINAL FUSION CAGES in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80102513139 and manufactured by ULRICH GMBH & CO.KG.. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Dec 26, 2027.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including AESCULAP AG, OSTEOMED S.A, 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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80102513139
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Registration Details
ANVISA Registration Number: 80102513139
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

GAIOLA TEZO™ TITÂNIO
Risk Class III

Registration Details

80102513139

25351771707202340

04718143000194

Company Information

Germany
PT: ALEMANHA

Dates and Status

Dec 04, 2023

26/12/2027

09/18/2025 19:00:01

GAIOLA TEZO™ TITÂNIO
Risk Class III

Registration Details

80102513139

25351771707202340

04718143000194

Dates and Status

Dec 04, 2023

26/12/2027

09/18/2025 19:00:01