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"Merotec" image guide tube - Taiwan Registration 27e37343f7ee48cbb17d44df4d99f81d

Access comprehensive regulatory information for "Merotec" image guide tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 27e37343f7ee48cbb17d44df4d99f81d 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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27e37343f7ee48cbb17d44df4d99f81d
Registration Details
Taiwan FDA Registration: 27e37343f7ee48cbb17d44df4d99f81d
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Device Details

"Merotec" image guide tube
TW: โ€œ้บฅๆด›ๆณฐๅ…‹โ€ๅฝฑๅƒๅฐŽๅผ•ๅฐŽ็ฎก
Risk Class 2
Cancelled

Registration Details

27e37343f7ee48cbb17d44df4d99f81d

DHA00602391306

Company Information

United States

Product Details

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

D Anesthesiology

D.5120 ้บป้†‰ๅ‚ณ่ผธๅฐŽ็ฎก

import

Dates and Status

Jul 31, 2012

Jul 31, 2022

Apr 12, 2024

Cancellation Information

Logged out

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