Taiwan FDA registration 8d99946626dff12c22c978f001f417f2

"Meikang" peritoneal dialysis catheters and accessories

TW: “美康”腹膜透析導管及配件
Taiwan flagTaiwan·Risk Class 2·Made (部分製程) in MEXICO;; MEDICAL COMPONENTS INC·Registered Sep 06, 2017 – Sep 06, 2027Active
Registration details
Analysis ID
8d99946626dff12c22c978f001f417f2
Customs Code
DHA05603021301
Company information
Manufacturer Country
Mexico;;United States
Authorized Representative
BAXTER HEALTHCARE LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
H Gastroenterology and urology
Product Type (Level 2)
H.5630 腹膜透析系統及其附件
Import Information
import
Dates and status
Registration Date
Sep 06, 2017
Expiry Date
Sep 06, 2027
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About this record

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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