Albumin Quantitative Testing Drug - Vietnam Registration 240000970/PCBB-HCM
Access comprehensive regulatory information for Albumin Quantitative Testing Drug in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TTBYT Loại B medical device is registered under number 240000970/PCBB-HCM and manufactured by Roche Diagnostics GmbH. The authorized representative in Vietnam is CÔNG TY TNHH ROCHE VIỆT NAM.
This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including Theo theo phụ lục, Theo phụ lục, and 5 recent registrations in the same category. Pure Global AI offers free access to 300,000+ Vietnamese medical device registrations, helping global MedTech companies navigate Vietnam MOH regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
Technical Details
In vitro testing used to quantify albumin in serum, plasma, urine, and cerebrospinal fluid (ratio of cerebrospinal fluid albumin/serum albumin) on the cobas and COBAS INTEGRA systems. The intended use of the specific applications for diagnosis Reiber*: In vitro testing used to quantify albumin in cerebrospinal fluid and corresponding serum/plasma in humans on the cobas systems. *Not available in all countries
Dates and Status
May 13, 2024
Albumin Quantitative Testing Drug
Fisher Diagnostics, A division of Fisher Scientific Company, LLC, A part of Thermo Fisher Scientific, Inc.
240002729/PCBB-HN
Microalbumin Quantitative Testing Drug
Finecare™ One Step MAU Rapid Quantitative Test
Guangzhou Wondfo Biotech Co., Ltd.
240002587/PCBB-HN
Albumin Quantitative Testing Drug
Roche Diagnostics GmbH
240000969/PCBB-HCM
Albumin Quantitative Testing Drug
Theo phụ lục
240000709/PCBB-HN
Albumin Quantitative Testing Drug
Theo phụ lục
240000711/PCBB-HN