Taiwan FDA registration c0a0bff000a1eb154668514ee13b3662
"Boss" Ear, nose, and throat manual surgical instrument (Non-Sterile)
TW: "伯斯" 耳鼻喉手動式外科器械 (未滅菌)
Taiwan·Risk Class 1·MD·BOSS INSTRUMENTS/INSTRUMED GMBH·Registered Aug 09, 2013 – Aug 09, 2018CancelledRegistration details
- Analysis ID
- c0a0bff000a1eb154668514ee13b3662
- License Form
- Ministry of Health Medical Device Import No. 013291
- Customs Code
- DHA09401329105
Company information
- Manufacturer
- BOSS INSTRUMENTS/INSTRUMED GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- FU TAI TRADING CO., LTD.
Product details
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G4420 OTOLARYNGARY Manual Surgical Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 09, 2013
- Expiry Date
- Aug 09, 2018
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Boss" Ear, nose, and throat manual surgical instrument (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c0a0bff000a1eb154668514ee13b3662 and manufactured by BOSS INSTRUMENTS/INSTRUMED GMBH. The authorized representative in Taiwan is FU TAI TRADING CO., LTD..
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