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"Mattens" pain-relieving gas supply - Taiwan Registration ec2380835a2786a0b5f21e83c01a1d66

Access comprehensive regulatory information for "Mattens" pain-relieving gas supply in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ec2380835a2786a0b5f21e83c01a1d66 and manufactured by MATRX BY MIDMARK. The authorized representative in Taiwan is YI LIN ENTERPRISE 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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ec2380835a2786a0b5f21e83c01a1d66
Registration Details
Taiwan FDA Registration: ec2380835a2786a0b5f21e83c01a1d66
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Device Details

"Mattens" pain-relieving gas supply
TW: "็‘ช็‰นๅธ"ๆญข็—›ๆฐฃ้ซ”ไพ›ๆ‡‰ๆฉŸ
Risk Class 2
Cancelled

Registration Details

ec2380835a2786a0b5f21e83c01a1d66

DHA00601771006

Company Information

United States

Product Details

For details, please refer to the approved version of Chinese copy

D Anesthesiology

D.5160 Anesthesia or analgesic gas supply machine

import

Dates and Status

Jan 22, 2007

Jan 22, 2012

Apr 30, 2014

Cancellation Information

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