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"Moritoka" acid-base tube (unsterilized) - Taiwan Registration 9cf2d0a1db8738d1435c1b384c23a0cf

Access comprehensive regulatory information for "Moritoka" acid-base tube (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9cf2d0a1db8738d1435c1b384c23a0cf and manufactured by SANDHILL SCIENTIFIC, INC.. The authorized representative in Taiwan is Kaiju Limited.

This page provides complete technical specifications, regulatory compliance details. 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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9cf2d0a1db8738d1435c1b384c23a0cf
Registration Details
Taiwan FDA Registration: 9cf2d0a1db8738d1435c1b384c23a0cf
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Device Details

"Moritoka" acid-base tube (unsterilized)
TW: "ๆฃฎๅพท่ณ€" ้…ธ้นผๆธฌ็ฎก (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

9cf2d0a1db8738d1435c1b384c23a0cf

DHA09401601700

Company Information

United States

Product Details

Limited to the first level identification range of the "pH electrode of the stomach (H.1400)" of the Measures for the Administration of Medical Devices.

H Gastroenterology and urology

H.1400 ่ƒƒ็š„้…ธ้นผๅบฆ้›ปๆฅต

Input;; QMS/QSD

Dates and Status

Dec 25, 2015

Dec 25, 2020

Nov 04, 2022

Cancellation Information

Logged out

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