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“ACCUTOME” Pachymeter - Taiwan Registration c261df64a2ae5fd7d6dabe8cc2c9b12d

Access comprehensive regulatory information for “ACCUTOME” Pachymeter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c261df64a2ae5fd7d6dabe8cc2c9b12d and manufactured by ACCUTOME, INC.. The authorized representative in Taiwan is BIOMEGA INSTRUMENT 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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c261df64a2ae5fd7d6dabe8cc2c9b12d
Registration Details
Taiwan FDA Registration: c261df64a2ae5fd7d6dabe8cc2c9b12d
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Device Details

“ACCUTOME” Pachymeter
TW: “愛可德”角膜厚度測量儀
Risk Class 2
MD
Cancelled

Registration Details

c261df64a2ae5fd7d6dabe8cc2c9b12d

Ministry of Health Medical Device Import No. 027614

DHA05602761409

Company Information

United States

Product Details

P Devices for radiology

P1560 ultrasonic echo imaging system

Imported from abroad

Dates and Status

Sep 02, 2015

Sep 02, 2020

Jun 16, 2022

Cancellation Information

Logged out

許可證已逾有效期未申請展延