“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.
Device Details
Registration Details
3837f80f8f01a86b91606c89c4d3b2ee
Ministry of Health Medical Device Import No. 025315
DHA05602531502
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

