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KOBAYASHI WARMER L (NON-STERILE) - Taiwan Registration d191871636ec5dee684e1a523c9431ee

Access comprehensive regulatory information for KOBAYASHI WARMER L (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 d191871636ec5dee684e1a523c9431ee and manufactured by KIRIBAI KOBAYASHI PHARMACEUTICAL CO., LTD., FUJIOKA FACTORY. The authorized representative in Taiwan is KOBAYASHI PHARMACEUTICAL (TAIWAN) CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including KIRIBAI KOBAYASHI PHARMACEUTICAL 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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d191871636ec5dee684e1a523c9431ee
Registration Details
Taiwan FDA Registration: d191871636ec5dee684e1a523c9431ee
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Device Details

KOBAYASHI WARMER L (NON-STERILE)
TW: ๅฐ็™ฝๅ…” ่ˆ’็ทฉๆบซ็†ฑ่ฒผ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

d191871636ec5dee684e1a523c9431ee

Ministry of Health Medical Device Import No. 022584

DHA09402258408

Product Details

Limited to the classification and grading management of medical equipment, the first level identification range of "Discardable Hot and Cold Compress Packs for Medical Use (O.5710)".

o Equipment for physical medicine

O5710 Discardable Hot and Cold Compress for Medical Use

Imported from abroad

Dates and Status

Jul 26, 2021

Jul 26, 2026

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