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)
Taiwan flagTaiwan·Risk Class 1·GIMMI GMBH.·Registered Apr 03, 2006 – Apr 03, 2026Expired
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