Taiwan FDA registration 2f7266f26858d7883596915b7bdb3ccc
"Albert Hess" Manual Eye Surgery Instruments (Unsterilized)
TW: "阿爾伯特赫斯" 手動式眼科手術器械 (未滅菌)
Taiwan·Risk Class 1·ALBERT HEISS GMBH & CO. KG·Registered Oct 31, 2011 – Oct 31, 2021CancelledRegistration details
- Analysis ID
- 2f7266f26858d7883596915b7bdb3ccc
- Customs Code
- DHA04401099201
Company information
- Manufacturer
- ALBERT HEISS GMBH & CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- RAY HUNG INSTRUMENT CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Eye Surgery Instruments (M.4350)".
- 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 31, 2011
- Expiry Date
- Oct 31, 2021
- Cancellation Date
- Oct 06, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Albert Hess" Manual Eye Surgery Instruments (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2f7266f26858d7883596915b7bdb3ccc and manufactured by ALBERT HEISS GMBH & CO. KG. The authorized representative in Taiwan is RAY HUNG INSTRUMENT 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