Taiwan FDA registration 0afb98dd1b79fbc29ec040f248a94363
LM Instruments SA NEBULIZER KIT AND ACCESSORY
TW: 因士徹曼 噴霧罐組及配件
Registration details
- Analysis ID
- 0afb98dd1b79fbc29ec040f248a94363
- License Form
- Ministry of Health Medical Device Manufacturing No. 005425
Company information
- Manufacturer
- HSINER CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- HSINER CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5630 Sprayer
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Aug 17, 2016
- Expiry Date
- Aug 17, 2026
About this record
Access comprehensive regulatory information for LM Instruments SA NEBULIZER KIT AND ACCESSORY in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0afb98dd1b79fbc29ec040f248a94363 and manufactured by HSINER CO., LTD.. The authorized representative in Taiwan is HSINER 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.
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