Taiwan FDA registration b7ecf4339ed8675d0a227f19081abf46
Ji Ji Le Al Fidalip Rigid laryngoscope (unsterilized)
TW: 吉銤 艾爾菲達力普 硬式喉頭鏡(未滅菌)
Registration details
- Analysis ID
- b7ecf4339ed8675d0a227f19081abf46
- Customs Code
- DHA04400342106
Company information
- Manufacturer
- GIMMI GMBH.
- Manufacturer Country
- Germany
- Authorized Representative
- GRAND MEDICAL INSTRUMENT CO., LTD.
Product details
- Intended Use
- Rigid laryngoscopy is a device used to examine and examine the patient's upper airway and assist in the placement of endotracheal intubation.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5540 Rigid laryngoscope
- Import Information
- import
Dates and status
- Registration Date
- Apr 03, 2006
- Expiry Date
- Apr 03, 2026
About this record
Access comprehensive regulatory information for Ji Ji Le Al Fidalip 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 b7ecf4339ed8675d0a227f19081abf46 and manufactured by GIMMI GMBH.. The authorized representative in Taiwan is GRAND MEDICAL INSTRUMENT 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