Taiwan FDA registration 0e485d3ee78a1295494893340bbff9a1
Goode eye surgical instruments
TW: 固德眼科手術器械
Registration details
- Analysis ID
- 0e485d3ee78a1295494893340bbff9a1
- Customs Code
- DHA04400387200
Company information
- Manufacturer
- HANS GEUDER GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- Meidcheng Instrument Co., Ltd
Product details
- 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
- Apr 14, 2006
- Expiry Date
- Apr 14, 2011
- Cancellation Date
- Nov 06, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Goode eye surgical instruments in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0e485d3ee78a1295494893340bbff9a1 and manufactured by HANS GEUDER GMBH. The authorized representative in Taiwan is Meidcheng 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.
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