Taiwan FDA registration b1d84eff219232294034703fb0644f7b
"Fubi" OTOLARYNG-throat manual surgical instrument (unsterile)
TW: "普美" 耳鼻喉手動式外科器械 (未滅菌)
Taiwan·Risk Class 1·PRO-MED INSTRUMENTE GMBH·Registered Mar 23, 2006 – Mar 23, 2011CancelledRegistration details
- Analysis ID
- b1d84eff219232294034703fb0644f7b
- Customs Code
- DHA04400309200
Company information
- Manufacturer
- PRO-MED INSTRUMENTE GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- WONDERFUL INSTRUMENTS COMPANY, LTD.
Product details
- Intended Use
- It is limited to the scope of first-level identification of the Administrative Measures for Medical Devices (Otolaryngology Manual Surgical Instruments [G.4420]).
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.4420 Otolaryngology manual surgical instruments
- Import Information
- import
Dates and status
- Registration Date
- Mar 23, 2006
- Expiry Date
- Mar 23, 2011
- Cancellation Date
- Jan 18, 2013
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Fubi" OTOLARYNG-throat manual surgical instrument (unsterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b1d84eff219232294034703fb0644f7b and manufactured by PRO-MED INSTRUMENTE GMBH. The authorized representative in Taiwan is WONDERFUL INSTRUMENTS COMPANY, LTD..
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