Pure Global

GASTRIN RELEASING PEPTIDE - ANVISA Registration 80102513397

Access comprehensive regulatory information for GASTRIN RELEASING PEPTIDE in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80102513397 and manufactured by AUTOBIO DIAGNOSTICS CO., LTD. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Apr 07, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 3 companies making the same product including ABBOTT GMBH, LABTEST DIAGNOSTICA 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
3 Competitors
5 Recent Registrations
80102513397
2 Related Devices
Registration Details
ANVISA Registration Number: 80102513397
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Related Devices (2)

Família AutoLumo Micropartículas G-17 (CLIA)
Risk Class III

Registration Details

80102513397

25351449737202453

04718143000194

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Apr 07, 2025

07/04/2035

09/18/2025 19:00:01

Família AutoLumo Micropartículas G-17 (CLIA)
Risk Class III

Registration Details

80102513397

25351449737202453

04718143000194

Dates and Status

Apr 07, 2025

07/04/2035

09/18/2025 19:00:01

Companies Making Similar Products
Top companies providing products with the same technical name: "GASTRIN RELEASING PEPTIDE"