Taiwan FDA registration 1b9b4cc31c97f75d333543ba6602af36
"Spiggle & Theis" Otoscope (Non-Sterile)
TW: "史賓格-席斯" 耳鏡 (未滅菌)
Taiwan·Risk Class 1·MD·SPIGGLE & THEIS MEDIZINTECHNIK GMBH·Registered Sep 19, 2017 – Sep 19, 2027ActiveRegistration details
- Analysis ID
- 1b9b4cc31c97f75d333543ba6602af36
- License Form
- Ministry of Health Medical Device Import No. 018328
- Customs Code
- DHA09401832801
Company information
- Manufacturer
- SPIGGLE & THEIS MEDIZINTECHNIK GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- GOLDENSPRING MEDI-TECH CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Otoscope (G.4770)".
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G4770 Otoscope
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 19, 2017
- Expiry Date
- Sep 19, 2027
About this record
Access comprehensive regulatory information for "Spiggle & Theis" Otoscope (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 1b9b4cc31c97f75d333543ba6602af36 and manufactured by SPIGGLE & THEIS MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is GOLDENSPRING MEDI-TECH CO., LTD..
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