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Teleflex Infant Nasal Breathing Device Tubing and Accessories (Unsterilized) - Taiwan Registration c3a473881836a294228b8dfa57cbd005

Access comprehensive regulatory information for Teleflex Infant Nasal Breathing Device Tubing and Accessories (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c3a473881836a294228b8dfa57cbd005 and manufactured by TELEFLEX MEDICAL. The authorized representative in Taiwan is BENQ MEDICAL TECHNOLOGY CORPORATION.

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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c3a473881836a294228b8dfa57cbd005
Registration Details
Taiwan FDA Registration: c3a473881836a294228b8dfa57cbd005
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Device Details

Teleflex Infant Nasal Breathing Device Tubing and Accessories (Unsterilized)
TW: โ€œๆณฐๅˆฉ็ฆโ€ๅฌฐๅ…’้ผปๅ‘ผๅธๅ™จ็ฎก่ทฏๅŠ้™„ไปถ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

c3a473881836a294228b8dfa57cbd005

DHA04401101504

Company Information

Mexico

Product Details

It is limited to the first level of identification of the medical device management measures "gas mask head strap (D.5560)" and "respirator tubing (D.5975)".

D Anesthesiology

D.5975 Respirator Tubing;; D.5560 Aerophyric mask head strap

import

Dates and Status

Nov 04, 2011

Nov 04, 2021

May 21, 2018

Cancellation Information

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