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"Khanma" warm chamber (unsterilized) - Taiwan Registration 1f80cd9b42e02c937da8c4239a6df25b

Access comprehensive regulatory information for "Khanma" warm chamber (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1f80cd9b42e02c937da8c4239a6df25b and manufactured by SHIAN JIA MEEI ENTERPRISE CO., LTD.. The authorized representative in Taiwan is SHIAN JIA MEEI ENTERPRISE CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SHIAN JIA MEEI ENTERPRISE CO., LTD., 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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1f80cd9b42e02c937da8c4239a6df25b
Registration Details
Taiwan FDA Registration: 1f80cd9b42e02c937da8c4239a6df25b
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Device Details

"Khanma" warm chamber (unsterilized)
TW: "ๆฑ—้ฆฌ" ๆบซ็†ฑ่‰™ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

1f80cd9b42e02c937da8c4239a6df25b

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Power Thermal Cushion (O.5740)".

o Physical Medical Sciences

O.5740 ๅ‹•ๅŠ›ๅผ็†ฑๆ•ทๅขŠ

ๅœ‹็”ข;; QMS/QSD

Dates and Status

Jul 25, 2016

Jul 25, 2026

Sep 30, 2021

Cancellation Information

Logged out

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