Taiwan FDA registration 254cefd5e29c3045ad181df813cf409e

"Alans" retractable needle lancet (unsterilized)

TW: "亞蘭斯"可退針式採血筆(未滅菌)
Taiwan flagTaiwan·Risk Class 1·SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD·Registered Mar 01, 2016 – Mar 01, 2021Cancelled
Registration details
Analysis ID
254cefd5e29c3045ad181df813cf409e
Customs Code
DHA09600265101
Company information
Manufacturer Country
China
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
Input;; Chinese goods
Dates and status
Registration Date
Mar 01, 2016
Expiry Date
Mar 01, 2021
Cancellation Date
Sep 23, 2023
Cancellation information
Status
Logged out
Reason
自行鍵入
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About this record

Access comprehensive regulatory information for "Alans" retractable needle lancet (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 254cefd5e29c3045ad181df813cf409e and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD. The authorized representative in Taiwan is ALLIANCE INTERNATIONAL MEDICAL CO., LTD..

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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