Taiwan FDA registration 4233934e01d31ffa0c0c9496140ead2f
"AnyCheck" Frequency Analyzer (non-sterile)
TW: "紐白測" 牙科植體穩定分析儀 (未滅菌)
Registration details
- Analysis ID
- 4233934e01d31ffa0c0c9496140ead2f
- License Form
- Ministry of Health Medical Device Import No. 018356
- Customs Code
- DHA09401835606
Company information
- Manufacturer
- NEOBIOTECH CO., LTD
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- NEOBIOTECH TAIWAN CO., LTD
Product details
- Intended Use
- Limited to the first level recognition range of medical equipment management measures dental handpieces and their accessories (F.4200).
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F4200 Dental Handpiece and its accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 27, 2017
- Expiry Date
- Sep 27, 2022
About this record
Access comprehensive regulatory information for "AnyCheck" Frequency Analyzer (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 4233934e01d31ffa0c0c9496140ead2f and manufactured by NEOBIOTECH CO., LTD. The authorized representative in Taiwan is NEOBIOTECH TAIWAN 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