Taiwan FDA registration 1a7b889b27bf846387b8f066f32d9cfa
“Simex” Subglottic aspiration system
TW: “賽麥斯”聲門下抽吸系統
Taiwan·Risk Class 2·MD·Simex Medizintechnik GmbH·Registered Jun 09, 2021 – Jun 09, 2026ExpiredRegistration details
- Analysis ID
- 1a7b889b27bf846387b8f066f32d9cfa
- License Form
- Ministry of Health Medical Device Import No. 034593
- Customs Code
- DHA05603459305
Company information
- Manufacturer
- Simex Medizintechnik GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- BIOSYSTEMS INC.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4780 powered suction pump
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 09, 2021
- Expiry Date
- Jun 09, 2026
About this record
Access comprehensive regulatory information for “Simex” Subglottic aspiration system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1a7b889b27bf846387b8f066f32d9cfa and manufactured by Simex Medizintechnik GmbH. The authorized representative in Taiwan is BIOSYSTEMS INC..
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