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Standard Calibration Solution for Sirolimus Quantification Testing - Vietnam Registration 2403217ĐKLH/BYT-HTTB

Access comprehensive regulatory information for Standard Calibration Solution for Sirolimus Quantification Testing in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TTBYT Loại C medical device is registered under number 2403217ĐKLH/BYT-HTTB and manufactured by Fujirebio Diagnostics, Inc.. The authorized representative in Vietnam is VĂN PHÒNG ĐẠI DIỆN ABBOTT LABORATORIES GMBH TẠI THÀNH PHỐ HÀ NỘI.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Fujirebio Diagnostics, Inc., and 1 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.

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2403217ĐKLH/BYT-HTTB
Registration Details
Vietnam MOH Registration: 2403217ĐKLH/BYT-HTTB
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Device Details

Standard Calibration Solution for Sirolimus Quantification Testing
VN: Chất hiệu chuẩn xét nghiệm định lượng Sirolimus
Risk Class TTBYT Loại C

Registration Details

2403217ĐKLH/BYT-HTTB

000.00.04.G18-230615-0002

ARCHITECT Sirolimus Calibrators

1L76-01

Technical Details

The ARCHITECT Sirolimus Calibrators are used to calibrate the ARCHITECT iSystem when performing quantitative analysis of sirolimus in the total blood of humans. For more information, refer to the Architect Sirolimus Assay Kit Manual and the Architect System Operations Manual.

Dates and Status

Nov 02, 2024

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