Taiwan FDA registration ade2b81c6c1bcdef9f5c89f6bffeaca1

"DenMat" Ophthalmic Operating Spectacles(loupes) (Non-Sterile)

TW: "登美" 眼科用手術眼鏡(放大鏡) (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·DENMAT HOLDINGS, LLC.·Registered Sep 10, 2013 – Sep 10, 2018Cancelled
Registration details
Analysis ID
ade2b81c6c1bcdef9f5c89f6bffeaca1
License Form
Ministry of Health Medical Device Import No. 013396
Customs Code
DHA09401339606
Company information
Manufacturer Country
United States
Authorized Representative
AIREX CORP.
Product details
Product Type (Level 1)
M Ophthalmic devices
Product Type (Level 2)
M4770 Ophthalmic surgical glasses (magnifying glasses)
Import Information
Imported from abroad
Dates and status
Registration Date
Sep 10, 2013
Expiry Date
Sep 10, 2018
Cancellation Date
May 19, 2022
Cancellation information
Status
Logged out
Reason
許可證逾有效期未申請展延
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About this record

Access comprehensive regulatory information for "DenMat" Ophthalmic Operating Spectacles(loupes) (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ade2b81c6c1bcdef9f5c89f6bffeaca1 and manufactured by DENMAT HOLDINGS, LLC.. The authorized representative in Taiwan is AIREX CORP..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including DENMAT HOLDINGS, LLC., DENMAT HOLDINGS, LLC, and 2 recent registrations in the same category. 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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