Taiwan FDA registration e23c306286630d498f1e181cf166639e
"Bedegram" uterine perfusion manipulation cannula
TW: “百脫克”子宮灌注操縱套管
Taiwan·Risk Class 2·Cemao Co., Ltd.;; BIOTEQUE AMERICA, INC·Registered Mar 26, 2020 – Mar 26, 2025ExpiredRegistration details
- Analysis ID
- e23c306286630d498f1e181cf166639e
- Customs Code
- DHA05500676801
Company information
- Manufacturer
- Cemao Co., Ltd.;; BIOTEQUE AMERICA, INC
- Manufacturer Country
- Taiwan, Province of China;;United States
- Authorized Representative
- RI-MING ENTERPRISES CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- l Obstetrics and Gynecology
- Product Type (Level 2)
- L.0002 Uterine manipulators/injection catheters
- Import Information
- Commissioned domestic manufacturing abroad, and then imported from abroad; Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Mar 26, 2020
- Expiry Date
- Mar 26, 2025
About this record
Access comprehensive regulatory information for "Bedegram" uterine perfusion manipulation cannula in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e23c306286630d498f1e181cf166639e and manufactured by Cemao Co., Ltd.;; BIOTEQUE AMERICA, INC. The authorized representative in Taiwan is RI-MING ENTERPRISES CO., LTD..
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