Taiwan FDA registration a4bcc84400d5f0badefa0cb5afcb59dc

"Shineteh" Manual surgical instrument for general use (Non-sterile)

TW: "信德" 一般手術用手動式器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·CEATEC MEDIZINTECHNIK GMBH·Registered Oct 23, 2020 – Oct 23, 2025Expired
Registration details
Analysis ID
a4bcc84400d5f0badefa0cb5afcb59dc
License Form
Ministry of Health Medical Device Import No. 022060
Customs Code
DHA09402206000
Company information
Manufacturer Country
Germany
Authorized Representative
SHINETEH INSTRUMENTS CO., LTD.
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
Product Type (Level 1)
I General and plastic surgical devices
Product Type (Level 2)
I4800 General Surgery Manual Instrument
Import Information
Imported from abroad
Dates and status
Registration Date
Oct 23, 2020
Expiry Date
Oct 23, 2025
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About this record

Access comprehensive regulatory information for "Shineteh" Manual surgical instrument for general use (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 a4bcc84400d5f0badefa0cb5afcb59dc and manufactured by CEATEC MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is SHINETEH INSTRUMENTS CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including CHR. DIENER GMBH & CO. KG, 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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