Taiwan FDA registration e767351b546543470843f7b63e929b2a

"Integra" Jarit instrument case (Non-Sterile)

TW: "殷特歌爾" 潔瑞器械盒 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·BAHADIR CORPORATION·Registered Jun 30, 2017 – Jun 30, 2022Expired
Registration details
Analysis ID
e767351b546543470843f7b63e929b2a
License Form
Ministry of Health Medical Device Import No. 018027
Customs Code
DHA09401802700
Company information
Manufacturer Country
Turkey
Authorized Representative
KINDMED CORPORATION
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
Jun 30, 2017
Expiry Date
Jun 30, 2022
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About this record

Access comprehensive regulatory information for "Integra" Jarit instrument case (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 e767351b546543470843f7b63e929b2a and manufactured by BAHADIR CORPORATION. The authorized representative in Taiwan is KINDMED CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including INTEGRA YORK PA, INC., 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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