Taiwan FDA registration 9c0783ee69dad95015001a136c3751f5

Fore Lancet (sterilized)

TW: 福爾 採血針 (滅菌)
Taiwan flagTaiwan·Risk Class 1·Qiaolian Technology Co., Ltd. Nankan No. 2 Factory·Registered Dec 01, 2015 – Dec 01, 2020Cancelled
Registration details
Analysis ID
9c0783ee69dad95015001a136c3751f5
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
TAIDOC TECHNOLOGY 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, Plastic Surgery and Dermatology
Product Type (Level 2)
I.4800 Hand Instruments for General Surgery
Import Information
QMS/QSD;; 國產;; 委託製造
Dates and status
Registration Date
Dec 01, 2015
Expiry Date
Dec 01, 2020
Cancellation Date
Aug 05, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for Fore Lancet (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9c0783ee69dad95015001a136c3751f5 and manufactured by Qiaolian Technology Co., Ltd. Nankan No. 2 Factory. The authorized representative in Taiwan is TAIDOC TECHNOLOGY CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BEIJING RUICHENG MEDICAL SUPPLIES 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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