Taiwan FDA registration 394e556f81422dbb59e9135235ede923
"STEMA" Non-Electric Biopsy Forceps (Non-Sterile)
TW: "思狄瑪"非電動活體組織夾(未滅菌)
Taiwan·Risk Class 1·MD·STEMA MEDIZINTECHNIK GMBH·Registered Jun 13, 2018 – Jun 13, 2023CancelledRegistration details
- Analysis ID
- 394e556f81422dbb59e9135235ede923
- License Form
- Ministry of Health Medical Device Import No. 019178
- Customs Code
- DHA09401917800
Company information
- Manufacturer
- STEMA MEDIZINTECHNIK GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- DERMACARE BIOMED INC.
Product details
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H1075 Gastroenterology - Urology biopsy instruments
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 13, 2018
- Expiry Date
- Jun 13, 2023
- Cancellation Date
- Jan 18, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "STEMA" Non-Electric Biopsy Forceps (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 394e556f81422dbb59e9135235ede923 and manufactured by STEMA MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is DERMACARE BIOMED INC..
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