Taiwan FDA registration 1e12f069136bde5594e743d344be5741
"Minimally invasive" foreign body forceps
TW: “微創”異物鉗
Taiwan·Risk Class 2·Micro-Tech (Nanjing) Co., Ltd.·Registered Jul 25, 2017 – Jul 25, 2022CancelledRegistration details
- Analysis ID
- 1e12f069136bde5594e743d344be5741
- Customs Code
- DHA09200082900
Company information
- Manufacturer
- Micro-Tech (Nanjing) Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- ERA BIOTEQ ENTERPRISE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Jul 25, 2017
- Expiry Date
- Jul 25, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Minimally invasive" foreign body forceps in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1e12f069136bde5594e743d344be5741 and manufactured by Micro-Tech (Nanjing) Co., Ltd.. The authorized representative in Taiwan is ERA BIOTEQ ENTERPRISE CO., LTD..
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