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"Sentinel" Cholinesterase Liquid (Non-Sterile) - Taiwan Registration b9110c5bd4354a0546bf65231845ab6b

Access comprehensive regulatory information for "Sentinel" Cholinesterase Liquid (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b9110c5bd4354a0546bf65231845ab6b and manufactured by SENTINEL CH. SPA. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.

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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b9110c5bd4354a0546bf65231845ab6b
Registration Details
Taiwan FDA Registration: b9110c5bd4354a0546bf65231845ab6b
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Device Details

"Sentinel" Cholinesterase Liquid (Non-Sterile)
TW: "่–ๆ่ซพ"่†ฝ้นผ่„‚้…ถ่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

b9110c5bd4354a0546bf65231845ab6b

Ministry of Health Medical Device Import No. 018345

DHA09401834501

Company Information

Italy

Product Details

Limited to the first level identification range of the bilisterase test system (A.3240) of the Measures for the Administration of Medical Devices.

A Clinical chemistry and clinical toxicology

A3240 Bilisterase Test System

Imported from abroad

Dates and Status

Sep 22, 2017

Sep 22, 2027