Taiwan FDA registration b1a82f606b120d2ca285849d5b0c05d4
“Keeler” Otoscopes (Non-Sterile)
TW: “奇勒” 耳鏡(未滅菌)
Taiwan·Risk Class 1·MD·Keeler Limited·Registered Mar 29, 2022 – Mar 29, 2027ActiveRegistration details
- Analysis ID
- b1a82f606b120d2ca285849d5b0c05d4
- License Form
- Ministry of Health Medical Device Import No. 022772
- Customs Code
- DHA09402277209
Company information
- Manufacturer
- Keeler Limited
- Manufacturer Country
- United Kingdom
- Authorized Representative
- EVERLIGHT 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)
- G4770 Otoscope
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 29, 2022
- Expiry Date
- Mar 29, 2027
About this record
Access comprehensive regulatory information for “Keeler” Otoscopes (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 b1a82f606b120d2ca285849d5b0c05d4 and manufactured by Keeler Limited. The authorized representative in Taiwan is EVERLIGHT 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