Taiwan FDA registration 35a67742dfcce89c13f2e83d43d25c53

"Bidi" manual eye surgery instruments

TW: 〝必帝〞手動式眼科手術器械
Taiwan flagTaiwan·Risk Class 1·BD OPHTHALMIC SYSTEMS·Registered Oct 28, 2005 – Oct 28, 2010Cancelled
Registration details
Analysis ID
35a67742dfcce89c13f2e83d43d25c53
Customs Code
DHA04400140501
Company information
Manufacturer Country
United States
Product details
Intended Use
Used to assist or perform eye surgery procedures.
Product Type (Level 1)
M Ophthalmology
Product Type (Level 2)
M.4350 手動式眼科手術器械
Import Information
import
Dates and status
Registration Date
Oct 28, 2005
Expiry Date
Oct 28, 2010
Cancellation Date
Oct 26, 2012
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
Companies making similar products

Top companies providing products similar to ""Bidi" manual eye surgery instruments"

Recent registrations

Recently registered similar products

About this record

Access comprehensive regulatory information for "Bidi" manual eye surgery instruments in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 35a67742dfcce89c13f2e83d43d25c53 and manufactured by BD OPHTHALMIC SYSTEMS. The authorized representative in Taiwan is Taiwan Branch of American Business Bidi Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BD OPHTHALMIC SYSTEMS, 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.

Free DatabasePowered by Pure Global AI89,000+ Devices1 Competitors1 Recent Registrations