Taiwan FDA registration 48a9c3c41950ceb43f950f2ac61a4cd7

Ophthalmic argon laser

TW: 眼科氬雷射儀
Taiwan flagTaiwan·COOPERVISION, INC., SURGICAL/SYSTEMS DIVISION·Registered Nov 01, 1985 – Nov 01, 1990Cancelled
Registration details
Analysis ID
48a9c3c41950ceb43f950f2ac61a4cd7
Customs Code
DHA00600390508
Company information
Manufacturer Country
United States
Authorized Representative
Huida Instruments Co., Ltd
Product details
Product Type (Level 1)
2101 Argon Laser Solidifier
Import Information
import
Dates and status
Registration Date
Nov 01, 1985
Expiry Date
Nov 01, 1990
Cancellation Date
Mar 11, 2005
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for Ophthalmic argon laser in Taiwan's medical device market through Pure Global AI's free database. is registered under number 48a9c3c41950ceb43f950f2ac61a4cd7 and manufactured by COOPERVISION, INC., SURGICAL/SYSTEMS DIVISION. The authorized representative in Taiwan is Huida Instruments Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including BRITT CORPORATION, G. RODENSTOCK INSTRUMENTE GMBH, and 2 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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