Taiwan FDA registration 43166fa2cd6985649dfa8d075884eac3

"ZEISS" ophthalmic medical laser system

TW: “蔡司”眼科醫療雷射系統
Taiwan flagTaiwan·Risk Class 2·CARL ZEISS MEDITEC AG·Registered Mar 24, 2020 – Mar 24, 2030Active
Registration details
Analysis ID
43166fa2cd6985649dfa8d075884eac3
Customs Code
DHA05603333007
Company information
Manufacturer Country
Germany
Authorized Representative
Carl Zeiss Co., Ltd. Taipei Branch
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.4392 後囊切除用Nd:YAG雷射
Import Information
import
Dates and status
Registration Date
Mar 24, 2020
Expiry Date
Mar 24, 2030
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About this record

Access comprehensive regulatory information for "ZEISS" ophthalmic medical laser system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 43166fa2cd6985649dfa8d075884eac3 and manufactured by CARL ZEISS MEDITEC AG. The authorized representative in Taiwan is Carl Zeiss Co., Ltd. Taipei Branch.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including CARL ZEISS MEDITEC AG, 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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