Taiwan FDA registration d038566432eb78ddfd75059f41123bd6

"Occolas" Ophthalmic Keratology (Unsterilized)

TW: "歐可樂斯" 眼科角膜儀 (未滅菌)

Taiwan·Risk Class 1·OCULUS OPTIKGERÄTE GMBH·Registered May 15, 2006 – May 15, 2026Cancelled

Registration details

Analysis ID: d038566432eb78ddfd75059f41123bd6
Customs Code: DHA04400448307

Company information

Manufacturer: OCULUS OPTIKGERÄTE GMBH
Manufacturer Country: Germany
Authorized Representative: TAIWAN HWA IN ENTERPRISE CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the "Corneatoscope (M.1350)" of the Measures for the Administration of Medical Devices.
Product Type (Level 1): M Ophthalmology
Product Type (Level 2): M.1350 Coratoscope
Import Information: import

Dates and status

Registration Date: May 15, 2006
Expiry Date: May 15, 2026
Cancellation Date: Sep 30, 2021

Cancellation information

Status: Logged out
Reason: 轉為登錄字號

About this record

Access comprehensive regulatory information for "Occolas" Ophthalmic Keratology (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d038566432eb78ddfd75059f41123bd6 and manufactured by OCULUS OPTIKGERÄTE GMBH. The authorized representative in Taiwan is TAIWAN HWA IN ENTERPRISE CO., LTD..

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