Taiwan FDA registration 42377d27658151534016e1682da4714d
"Bidi" ophthalmic catheters and peripheral accessories
TW: "必帝" 眼用導管及週邊配件
Taiwan·Risk Class 1·BD OPHTHALMIC SYSTEMS·Registered Feb 22, 2006 – Feb 22, 2011CancelledRegistration details
- Analysis ID
- 42377d27658151534016e1682da4714d
- Customs Code
- DHA04400270301
Company information
- Manufacturer
- BD OPHTHALMIC SYSTEMS
- Manufacturer Country
- United Kingdom
- Authorized Representative
- Taiwan Branch of American Business Bidi Co., Ltd
Product details
- Intended Use
- Non-electric, hand-held devices used to assist or perform eye surgery.
- 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
- Feb 22, 2006
- Expiry Date
- Feb 22, 2011
- Cancellation Date
- Jun 10, 2011
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Bidi" ophthalmic catheters and peripheral accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 42377d27658151534016e1682da4714d 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. 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+ Devices