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"SMEK" Cold Light Meter (Unsterilized) - Taiwan Registration bdc0e08877943b140b2ac019c6451670

Access comprehensive regulatory information for "SMEK" 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 bdc0e08877943b140b2ac019c6451670 and manufactured by Spectral Medical Inc.. The authorized representative in Taiwan is HI-CLEARANCE INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Spectral Medical Inc., 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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bdc0e08877943b140b2ac019c6451670
Registration Details
Taiwan FDA Registration: bdc0e08877943b140b2ac019c6451670
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Device Details

"SMEK" Cold Light Meter (Unsterilized)
TW: โ€œๆ€้‚ๅ…‹โ€ๅ†ทๅ…‰ๅ„€ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

bdc0e08877943b140b2ac019c6451670

DHA08402149406

Company Information

Canada

Product Details

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

A Clinical chemistry and clinical toxicology

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

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Oct 01, 2021

Oct 31, 2025

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