Taiwan FDA registration 481e07af71208eb2e6a40c2a9dfaccae
"MAXER" Laryngostroboscope (Non-Sterile)
TW: "麥克斯爾" 喉頭閃頻內視鏡 (未滅菌)
Taiwan·Risk Class 1·MD·MAXER MEDIZINTECHNIK GMBH·Registered Dec 06, 2018 – Dec 06, 2023ExpiredRegistration details
- Analysis ID
- 481e07af71208eb2e6a40c2a9dfaccae
- License Form
- Ministry of Health Medical Device Import No. 019893
- Customs Code
- DHA09401989301
Company information
- Manufacturer
- MAXER MEDIZINTECHNIK GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- HIGH TOP MEDICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Laryngeal Flash Endoscopy (G.4750)".
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G4750 Laryngeal flash endoscope
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 06, 2018
- Expiry Date
- Dec 06, 2023
About this record
Access comprehensive regulatory information for "MAXER" Laryngostroboscope (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 481e07af71208eb2e6a40c2a9dfaccae and manufactured by MAXER MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is HIGH TOP MEDICAL CO., LTD..
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