Taiwan FDA registration 30e589d8366d88f3bb919dff2bbe665e

"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 Dec 27, 2005 – Dec 27, 2010Cancelled
Registration details
Analysis ID
30e589d8366d88f3bb919dff2bbe665e
Customs Code
DHA04400237902
Company information
Manufacturer Country
United States
Product details
Intended Use
Non-electric, hand-held devices used to assist or perform eye surgery.
Product Type (Level 1)
M Ophthalmology
Import Information
import
Dates and status
Registration Date
Dec 27, 2005
Expiry Date
Dec 27, 2010
Cancellation Date
Oct 26, 2012
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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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 30e589d8366d88f3bb919dff2bbe665e 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.

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