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“Myelotec” Flexible Fiberoptic Endoscope & Access Kits - Taiwan Registration 3837f80f8f01a86b91606c89c4d3b2ee

Access comprehensive regulatory information for “Myelotec” Flexible Fiberoptic Endoscope & Access Kits in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3837f80f8f01a86b91606c89c4d3b2ee and manufactured by MYELOTEC, INC.. The authorized representative in Taiwan is REVO LASER CORPORATION.

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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3837f80f8f01a86b91606c89c4d3b2ee
Registration Details
Taiwan FDA Registration: 3837f80f8f01a86b91606c89c4d3b2ee
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Device Details

“Myelotec” Flexible Fiberoptic Endoscope & Access Kits
TW: “麥洛泰克”軟式光纖內視鏡及其附件
Risk Class 2
MD
Cancelled

Registration Details

3837f80f8f01a86b91606c89c4d3b2ee

Ministry of Health Medical Device Import No. 025315

DHA05602531502

Company Information

United States

Product Details

N Orthopedic devices

N1100 Arthroscopy

Imported from abroad

Dates and Status

Aug 01, 2013

Aug 01, 2018

Jun 22, 2022

Cancellation Information

Logged out

許可證已逾有效期