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“Medi-Life” A.V. Fistula needle sets - Taiwan Registration 1c13e1bad7ac0314f5c78f51d2c80af2

Access comprehensive regulatory information for “Medi-Life” A.V. Fistula needle sets in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1c13e1bad7ac0314f5c78f51d2c80af2 and manufactured by Perfect Medical Industry (VN) Co., Ltd.. The authorized representative in Taiwan is MEDI-LIFE 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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1c13e1bad7ac0314f5c78f51d2c80af2
Registration Details
Taiwan FDA Registration: 1c13e1bad7ac0314f5c78f51d2c80af2
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Device Details

“Medi-Life” A.V. Fistula needle sets
TW: “美德來”內瘻管翼狀針
Risk Class 2
MD

Registration Details

1c13e1bad7ac0314f5c78f51d2c80af2

Ministry of Health Medical Device Import No. 030993

DHA05603099301

Company Information

Product Details

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

H Gastroenterology-urology devices

H5540 Blood access devices and accessories

Imported from abroad

Dates and Status

Mar 22, 2018

Mar 22, 2028