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"SMEK" Cold Light Meter (Unsterilized) - Taiwan Registration d0bdad625831444e356645d3f1e3a60b

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 d0bdad625831444e356645d3f1e3a60b 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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d0bdad625831444e356645d3f1e3a60b
Registration Details
Taiwan FDA Registration: d0bdad625831444e356645d3f1e3a60b
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Device Details

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

Registration Details

d0bdad625831444e356645d3f1e3a60b

DHA09402149402

Company Information

Canada

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

Input;; QMS/QSD

Dates and Status

Apr 29, 2020

Apr 29, 2025

Sep 30, 2021

Cancellation Information

Logged out

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