Taiwan FDA registration 22630dd913364500dceb7ada81184b8e

“Rexxam” Ophthalmic Refractometer (Non-Sterile)

TW: “隆祥”眼科用驗光機 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·REXXAM CO., LTD. KAGAWA FACTORY·Registered Feb 02, 2021 – Feb 02, 2026Cancelled
Registration details
Analysis ID
22630dd913364500dceb7ada81184b8e
License Form
Ministry of Health Medical Device Import No. 022286
Customs Code
DHA09402228600
Company information
Manufacturer Country
Japan
Authorized Representative
TAIWAN INSTRUMENT CO., LTD.
Product details
Product Type (Level 1)
M Ophthalmic devices
Product Type (Level 2)
M1760 Ophthalmic Refractive Machine
Import Information
Imported from abroad
Dates and status
Registration Date
Feb 02, 2021
Expiry Date
Feb 02, 2026
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

Access comprehensive regulatory information for “Rexxam” Ophthalmic Refractometer (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 22630dd913364500dceb7ada81184b8e and manufactured by REXXAM CO., LTD. KAGAWA FACTORY. The authorized representative in Taiwan is TAIWAN INSTRUMENT CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including REXXAM CO., LTD. KAGAWA FACTORY, and 1 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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