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"Smith" amniocentesis needle - Taiwan Registration 8498bf3a609424752f4f798e388130d6

Access comprehensive regulatory information for "Smith" amniocentesis needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8498bf3a609424752f4f798e388130d6 and manufactured by SMITHS MEDICAL INTERNATIONAL LTD.. The authorized representative in Taiwan is CEMMA 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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8498bf3a609424752f4f798e388130d6
Registration Details
Taiwan FDA Registration: 8498bf3a609424752f4f798e388130d6
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Device Details

"Smith" amniocentesis needle
TW: "ๅฒๅฏ†ๆ–ฏ"็พŠ่†œ็ฉฟๅˆบ้‡
Risk Class 1
Cancelled

Registration Details

8498bf3a609424752f4f798e388130d6

DHA04400237102

Company Information

United Kingdom

Product Details

Amniotic fluid sampler, which is used to diagnose pre-delivery congenital anomalies during 16-18 weeks of pregnancy and at any time after 24 weeks of pregnancy to assess fetal maturity.

l Obstetrics and Gynecology

import

Dates and Status

Dec 27, 2005

Dec 27, 2010

Nov 09, 2012

Cancellation Information

Logged out

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