Taiwan FDA registration 880a96a3651b054dbcf44201285a39c5

"Kersyth" dynamic meibomian gland scanning imager

TW: “題爾賽斯”動態瞼板腺掃描成像儀

Taiwan·Risk Class 2·TearScience, Inc.;; SPARTRONICS STRONGSVILLE Inc.·Registered May 26, 2018 – May 26, 2028Active

Registration details

Analysis ID: 880a96a3651b054dbcf44201285a39c5
Customs Code: DHA05603090402

Company information

Manufacturer: TearScience, Inc.;; SPARTRONICS STRONGSVILLE Inc.
Manufacturer Country: United States
Authorized Representative: AMO ASIA LIMITED, TAIWAN BRANCH (HONG KONG)

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): M Ophthalmology
Product Type (Level 2): M.1120 Ophthalmic camera
Import Information: import

Dates and status

Registration Date: May 26, 2018
Expiry Date: May 26, 2028

About this record

Access comprehensive regulatory information for "Kersyth" dynamic meibomian gland scanning imager in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 880a96a3651b054dbcf44201285a39c5 and manufactured by TearScience, Inc.;; SPARTRONICS STRONGSVILLE Inc.. The authorized representative in Taiwan is AMO ASIA LIMITED, TAIWAN BRANCH (HONG KONG).

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