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"Meikang" peritoneal dialysis catheters and accessories - Taiwan Registration 8d99946626dff12c22c978f001f417f2

Access comprehensive regulatory information for "Meikang" peritoneal dialysis catheters and accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8d99946626dff12c22c978f001f417f2 and manufactured by Made (部分製程) in MEXICO;; MEDICAL COMPONENTS INC. The authorized representative in Taiwan is BAXTER HEALTHCARE LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Made (部分製程) in MEXICO;; MEDICAL COMPONENTS INC, 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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8d99946626dff12c22c978f001f417f2
Registration Details
Taiwan FDA Registration: 8d99946626dff12c22c978f001f417f2
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Device Details

"Meikang" peritoneal dialysis catheters and accessories
TW: “美康”腹膜透析導管及配件
Risk Class 2

Registration Details

8d99946626dff12c22c978f001f417f2

DHA05603021301

Company Information

Product Details

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

H Gastroenterology and urology

H.5630 腹膜透析系統及其附件

import

Dates and Status

Sep 06, 2017

Sep 06, 2027

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