Taiwan FDA registration 9cf3931ebc2345cc91ba30fb4654ca55
"Anjibi" ENT manual surgical instruments (unsterilized)
TW: 〝安吉必〞耳鼻喉手動式手術器械 (未滅菌)
Taiwan·Risk Class 1·MGB ENDOSCOPIC DEVICES GMBH BERLIN·Registered May 06, 2009 – May 06, 2014CancelledRegistration details
- Analysis ID
- 9cf3931ebc2345cc91ba30fb4654ca55
- Customs Code
- DHA04400769804
Company information
- Manufacturer
- MGB ENDOSCOPIC DEVICES GMBH BERLIN
- Manufacturer Country
- Germany
- Authorized Representative
- HURRAYBIO CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT 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
- May 06, 2009
- Expiry Date
- May 06, 2014
- Cancellation Date
- Dec 14, 2016
Cancellation information
- Status
- Logged out
- Reason
- 屆期未申請展延
About this record
Access comprehensive regulatory information for "Anjibi" ENT manual surgical 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 9cf3931ebc2345cc91ba30fb4654ca55 and manufactured by MGB ENDOSCOPIC DEVICES GMBH BERLIN. The authorized representative in Taiwan is HURRAYBIO CO., LTD..
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