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"LDR" Manual surgical instrument for general use (Non-Sterile) - Taiwan Registration bcfa4de5656892a6d8fbd1eb98d450aa

Access comprehensive regulatory information for "LDR" Manual surgical instrument for general use (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 bcfa4de5656892a6d8fbd1eb98d450aa and manufactured by LDR MEDICAL. The authorized representative in Taiwan is HOLLING BIO-PHARMA. CORP..

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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bcfa4de5656892a6d8fbd1eb98d450aa
Registration Details
Taiwan FDA Registration: bcfa4de5656892a6d8fbd1eb98d450aa
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Device Details

"LDR" Manual surgical instrument for general use (Non-Sterile)
TW: "ๆจ‚่ฟช็ˆพ" ไธ€่ˆฌๆ‰‹่ก“็”จๆ‰‹ๅ‹•ๅผๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

bcfa4de5656892a6d8fbd1eb98d450aa

Ministry of Health Medical Device Import No. 013908

DHA09401390807

Company Information

France

Product Details

I General and plastic surgical devices

I4800 General Surgery Manual Instrument

Imported from abroad

Dates and Status

Mar 04, 2014

Mar 04, 2019

Jun 07, 2022

Cancellation Information

Logged out

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