Visit us at Medica, Dusseldorf, Germany 17-20 November 2025 at Hall 16, Stand D17-5 and ask us about our free AI tools and the document builder.
Pure Global

Probes - ANVISA Registration 10160619021

Access comprehensive regulatory information for Probes in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10160619021 and manufactured by STERIMED SURGICALS INDIA PVT. LTD.. The registration is held by INJEX INDÚSTRIAS CIRÚRGICAS 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 WELL LEAD MEDICAL CO, LTD, FRESENIUS KABI AG, 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
5 Competitors
5 Recent Registrations
10160619021
Registration Details
ANVISA Registration Number: 10160619021
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

SONDA FOLEY - INJEX
Risk Class II

Registration Details

10160619021

25351637991202245

59309302000199

Company Information

India
PT: ÍNDIA

Dates and Status

Dec 26, 2022

VIGENTE

09/18/2025 19:00:01