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PEPSINOGEN I - ANVISA Registration 80091010028

Access comprehensive regulatory information for PEPSINOGEN I in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80091010028 and manufactured by RD BIOMED LIMITED. The registration is held by UNISCOPE COM. IMP. E EXP. DE APARELHOS MED. HOSP. 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 ABBOTT GMBH, BIOHIT OYJ, 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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80091010028
Registration Details
ANVISA Registration Number: 80091010028
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Device Details

PEPTEST KIT
Risk Class II

Registration Details

80091010028

25351669826201471

02954483000199

Company Information

RD BIOMED LIMITED
United Kingdom
PT: REINO UNIDO

Dates and Status

Feb 02, 2015

VIGENTE

09/18/2025 19:00:01