Taiwan FDA registration aacedc80267d397fb984101b65861ac0
“PENTAX MEDICAL” VIDEO BRONCHOSCOPE
TW: “賓得醫療”電子式支氣管鏡
Taiwan·Risk Class 2·MD·HOYA CORPORATION PENTAX MIYAGI FACTORY·Registered Sep 30, 2017 – Sep 30, 2027ActiveRegistration details
- Analysis ID
- aacedc80267d397fb984101b65861ac0
- License Form
- Ministry of Health Medical Device Import No. 030319
- Customs Code
- DHA05603031904
Company information
- Manufacturer
- HOYA CORPORATION PENTAX MIYAGI FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- PENTAX MEDICAL SINGAPORE PTE. LTD. TAIWAN BRANCH(SINGAPORE)
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G4680 Bronchoscope (soft or rigid) and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 30, 2017
- Expiry Date
- Sep 30, 2027
About this record
Access comprehensive regulatory information for “PENTAX MEDICAL” VIDEO BRONCHOSCOPE in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number aacedc80267d397fb984101b65861ac0 and manufactured by HOYA CORPORATION PENTAX MIYAGI FACTORY. The authorized representative in Taiwan is PENTAX MEDICAL SINGAPORE PTE. LTD. TAIWAN BRANCH(SINGAPORE).
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