Taiwan FDA registration 3a79752458d3fe27f089a920d8e27417
"Albert Hayes" Manual Eye Surgery Instruments (Unsterilized)
TW: “艾伯特海斯”手動式眼科手術器械(未滅菌)
Registration details
- Analysis ID
- 3a79752458d3fe27f089a920d8e27417
- Customs Code
- DHA04400934609
Company information
- Manufacturer
- ALBERT HEISS GMBH & CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- VISIONRISE ENTERPRISE 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 11, 2010
- Expiry Date
- Oct 11, 2015
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Albert Hayes" 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 3a79752458d3fe27f089a920d8e27417 and manufactured by ALBERT HEISS GMBH & CO. KG. The authorized representative in Taiwan is VISIONRISE ENTERPRISE 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