Taiwan FDA registration 44756b5234fa6c0deeb41fa9332b45c9
"HORIZON" Rigid laryngoscope (Non-Sterile)
TW: "和豐" 硬式喉頭鏡 (未滅菌)
Registration details
- Analysis ID
- 44756b5234fa6c0deeb41fa9332b45c9
- License Form
- Ministry of Health Medical Device Import No. 019941
- Customs Code
- DHA09401994109
Company information
- Manufacturer
- QURESHI MANUFACTURING CORPORATION
- Manufacturer Country
- Pakistan
- Authorized Representative
- HORIZON INSTRUMENTS CO. ,LTD.
Product details
- Intended Use
- Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Rigid Laryngoscopy (D.5540)".
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5540 Rigid laryngoscope
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 20, 2018
- Expiry Date
- Dec 20, 2023
About this record
Access comprehensive regulatory information for "HORIZON" Rigid laryngoscope (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 44756b5234fa6c0deeb41fa9332b45c9 and manufactured by QURESHI MANUFACTURING CORPORATION. The authorized representative in Taiwan is HORIZON INSTRUMENTS CO. ,LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices