Taiwan FDA registration fa335838d8a122dc7e2c898a01af261d
"Midmark" Central Vacuum (Non-Sterile)
TW: "名馬克" 中央負壓機(未滅菌)
Taiwan·Risk Class 1·MD·MIDMARK CORPORATION·Registered Jun 12, 2018 – Jun 12, 2023ExpiredRegistration details
- Analysis ID
- fa335838d8a122dc7e2c898a01af261d
- License Form
- Ministry of Health Medical Device Import No. 019168
- Customs Code
- DHA09401916800
Company information
- Manufacturer
- MIDMARK CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- KOLN BIO-MEDICAL CO.,LTD
Product details
- Intended Use
- Limited to the first level identification range of dental surgical devices and their accessories (F.6640) under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F6640 Dental Surgical Devices and Their Accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 12, 2018
- Expiry Date
- Jun 12, 2023
About this record
Access comprehensive regulatory information for "Midmark" Central Vacuum (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 fa335838d8a122dc7e2c898a01af261d and manufactured by MIDMARK CORPORATION. The authorized representative in Taiwan is KOLN BIO-MEDICAL CO.,LTD.
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