Taiwan FDA registration f6938b11c84b1bc4ae5976af8de095d4

"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·INTEGRA YORK PA, INC.·Registered Mar 03, 2016 – Mar 03, 2021Expired
Registration details
Analysis ID
f6938b11c84b1bc4ae5976af8de095d4
License Form
Ministry of Health Medical Device Import No. 016226
Customs Code
DHA09401622609
Company information
Manufacturer Country
United States
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
Mar 03, 2016
Expiry Date
Mar 03, 2021
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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 f6938b11c84b1bc4ae5976af8de095d4 and manufactured by INTEGRA YORK PA, INC.. The authorized representative in Taiwan is KINDMED CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BAHADIR CORPORATION, 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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