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"Fujifilm" silicone self-catheter - Taiwan Registration e63720afcf569570f5debc9542bdd40c

Access comprehensive regulatory information for "Fujifilm" silicone self-catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e63720afcf569570f5debc9542bdd40c and manufactured by Fuji Systems Corporation, Shirakawa Plant. The authorized representative in Taiwan is MING HWAY TRADING 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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e63720afcf569570f5debc9542bdd40c
Registration Details
Taiwan FDA Registration: e63720afcf569570f5debc9542bdd40c
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Device Details

"Fujifilm" silicone self-catheter
TW: "ๅฏŒๅฃซ"็Ÿฝ่† ่‡ช่กŒๅฐŽๅฐฟ็ฎก
Risk Class 2

Registration Details

e63720afcf569570f5debc9542bdd40c

DHA00601685501

Company Information

Product Details

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

H Gastroenterology and urology

H.5250 Urine Collector and Accessories Thereof

import

Dates and Status

Jul 10, 2006

Jul 10, 2026