Taiwan FDA registration 6a9b7c512cb776602bd040c9363db284
"Heinyon" rigid laryngoscope (unsterilized)
TW: "海尼恩" 硬式喉頭鏡 (未滅菌)
Registration details
- Analysis ID
- 6a9b7c512cb776602bd040c9363db284
- Customs Code
- DHA04400985800
Company information
- Manufacturer
- HEINE OPTOTECHNIK GMBH & CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- DENSO SCIENTIFIC CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "rigid laryngoscope (D.5540)" of the Measures for the Classification and Grading Management of Medical Devices.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5540 Rigid laryngoscope
- Import Information
- import
Dates and status
- Registration Date
- Jan 26, 2011
- Expiry Date
- Jan 26, 2026
About this record
Access comprehensive regulatory information for "Heinyon" rigid laryngoscope (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6a9b7c512cb776602bd040c9363db284 and manufactured by HEINE OPTOTECHNIK GMBH & CO. KG. The authorized representative in Taiwan is DENSO SCIENTIFIC 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