Taiwan FDA registration e8be7fc2a79113592e7c22bf53289309
"Gisper" otoscopy (unsterilized)
TW: “吉銤”耳鏡(未滅菌）
Taiwan·Risk Class 1·GIMMI GMBH.·Registered Aug 25, 2010 – Aug 25, 2025ExpiredRegistration details
- Analysis ID
- e8be7fc2a79113592e7c22bf53289309
- Customs Code
- DHA04400913002
Company information
- Manufacturer
- GIMMI GMBH.
- Manufacturer Country
- Germany
- Authorized Representative
- GRAND MEDICAL INSTRUMENT CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "Otoscope (G.4770)" of the Administrative Measures for the Classification and Grading of Medical Equipment.
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.4770 Ear Mirrors
- Import Information
- import
Dates and status
- Registration Date
- Aug 25, 2010
- Expiry Date
- Aug 25, 2025
About this record
Access comprehensive regulatory information for "Gisper" otoscopy (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e8be7fc2a79113592e7c22bf53289309 and manufactured by GIMMI GMBH.. The authorized representative in Taiwan is GRAND MEDICAL INSTRUMENT CO., LTD..
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