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"Baqi" Bayer Flexion Cold Light Meter (Unsterilized) - Taiwan Registration 3b295c2c81d728e6d7a2843715727d82

Access comprehensive regulatory information for "Baqi" Bayer Flexion Cold Light Meter (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3b295c2c81d728e6d7a2843715727d82 and manufactured by BIOKIT, S.A.. The authorized representative in Taiwan is TRUGENE DIAGNOSTICS, INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BIOKIT, S.A., and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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3b295c2c81d728e6d7a2843715727d82
Registration Details
Taiwan FDA Registration: 3b295c2c81d728e6d7a2843715727d82
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Device Details

"Baqi" Bayer Flexion Cold Light Meter (Unsterilized)
TW: โ€œ็™พๅฅ‡โ€ๆ‹œ็ˆพๅฏŒไพ†่ฟ…ๅ†ทๅ…‰ๅ„€ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

3b295c2c81d728e6d7a2843715727d82

DHA04401249204

Company Information

Spain

Product Details

Limited to the first level identification range of "Colorimeter, Photometer or Spectrophotometer for Clinical Use (A.2300)" under the Measures for the Administration of Medical Devices.

A Clinical chemistry and clinical toxicology

A.2300 Colorimeter, photometer, or spectrophotometer for clinical use

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Dec 17, 2012

Dec 17, 2022

Sep 30, 2021

Cancellation Information

Logged out

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