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"Alans" lancet (sterilized) - Taiwan Registration 87d73cf7e839eed668b5cd9149184fdc

Access comprehensive regulatory information for "Alans" 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 87d73cf7e839eed668b5cd9149184fdc 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. 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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87d73cf7e839eed668b5cd9149184fdc
Registration Details
Taiwan FDA Registration: 87d73cf7e839eed668b5cd9149184fdc
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Device Details

"Alans" lancet (sterilized)
TW: "ไบž่˜ญๆ–ฏ" ๆŽก่ก€้‡ (ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

87d73cf7e839eed668b5cd9149184fdc

DHA09600296600

Company Information

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".

I General, Plastic Surgery and Dermatology

I.4800 Hand Instruments for General Surgery

Chinese goods;; input

Dates and Status

Jan 10, 2017

Jan 10, 2022

Apr 12, 2024

Cancellation Information

Logged out

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