Taiwan FDA registration 467cd95b17adbb89da556d5faac528f5

"ZEISS" hydrophobic posterior chamber intraocular lens

TW: “蔡司” 疏水性後房人工水晶體

Taiwan·Risk Class 3·CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec Production, LLC.·Registered Feb 01, 2024 – Feb 01, 2029Active

Registration details

Analysis ID: 467cd95b17adbb89da556d5faac528f5
Customs Code: DHA05603691307

Company information

Manufacturer: CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec Production, LLC.
Manufacturer Country: United States;;Germany
Authorized Representative: Carl Zeiss Co., Ltd. Taipei Branch

Product details

Intended Use: Details are as detailed as approved Chinese instructions
Product Type (Level 1): M Ophthalmology
Product Type (Level 2): M.3600 Artificial Crystal
Import Information: Input;; Contract manufacturing

Dates and status

Registration Date: Feb 01, 2024
Expiry Date: Feb 01, 2029

About this record

Access comprehensive regulatory information for "ZEISS" hydrophobic posterior chamber intraocular lens in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 467cd95b17adbb89da556d5faac528f5 and manufactured by CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec Production, LLC.. The authorized representative in Taiwan is Carl Zeiss Co., Ltd. Taipei Branch.

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