Taiwan FDA registration 4f3d51108df8ad150bb896837938c8ac
"LM" Dental Hand Instrument (Non-Sterile)
TW: "雷門" 牙科手用器械 (未滅菌)
Taiwan·Risk Class 1·MD·LM-INSTRUMENTS OY·Registered Apr 16, 2015 – Apr 16, 2020CancelledRegistration details
- Analysis ID
- 4f3d51108df8ad150bb896837938c8ac
- License Form
- Ministry of Health Medical Device Import No. 015118
- Customs Code
- DHA09401511801
Company information
- Manufacturer
- LM-INSTRUMENTS OY
- Manufacturer Country
- Finland
- Authorized Representative
- FRANKFURT TECHNOLOGY CO., LTD.
Product details
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F4565 Hand instruments for dental use
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 16, 2015
- Expiry Date
- Apr 16, 2020
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "LM" Dental Hand Instrument (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 4f3d51108df8ad150bb896837938c8ac and manufactured by LM-INSTRUMENTS OY. The authorized representative in Taiwan is FRANKFURT TECHNOLOGY 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