Taiwan FDA registration ddf42a6dcf0c37bc0a1b956bde359af6

"ZEISS" ophthalmic laser system

TW: “蔡司” 眼科醫療雷射系統
Taiwan flagTaiwan·Risk Class 2·CARL ZEISS MEDITEC AG·Registered Nov 14, 2023 – Nov 14, 2028Active
Registration details
Analysis ID
ddf42a6dcf0c37bc0a1b956bde359af6
Customs Code
DHA05603675706
Company information
Manufacturer Country
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.4390 眼科雷射裝置
Import Information
import
Dates and status
Registration Date
Nov 14, 2023
Expiry Date
Nov 14, 2028
Companies making similar products

Top companies providing products similar to ""ZEISS" ophthalmic laser system"

Recent registrations

Recently registered similar products

About this record

Access comprehensive regulatory information for "ZEISS" ophthalmic 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 ddf42a6dcf0c37bc0a1b956bde359af6 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 4 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.

Free DatabasePowered by Pure Global AI89,000+ Devices1 Competitors4 Recent Registrations