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"Telifano" Epidural anesthesia catheter kit - Taiwan Registration 6f39dd6eade588122c8571d69268ffd0

Access comprehensive regulatory information for "Telifano" Epidural anesthesia catheter kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6f39dd6eade588122c8571d69268ffd0 and manufactured by Arrow International C.R. a.s.;; Arrow International LLC(Subsidiary of Teleflex Incorporated). The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Arrow Internacional de Chihuahua de S.A. de C.V.;; Arrow International LLC (Subsidiary of Teleflex Incorporated), 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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6f39dd6eade588122c8571d69268ffd0
Registration Details
Taiwan FDA Registration: 6f39dd6eade588122c8571d69268ffd0
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Device Details

"Telifano" Epidural anesthesia catheter kit
TW: โ€œๆณฐๅˆฉ็ฆไบž่ซพโ€ ็กฌ่„Š่†œๅค–้บป้†‰ๅฐŽ็ฎกๅฅ—็ต„
Risk Class 2

Registration Details

6f39dd6eade588122c8571d69268ffd0

DHA05603071002

Product Details

For details, it is Chinese approved copy of the imitation order

D Anesthesiology

D.5120 ้บป้†‰ๅ‚ณ่ผธๅฐŽ็ฎก

Input;; Contract manufacturing

Dates and Status

Jan 18, 2018

Jan 18, 2028

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