Taiwan FDA registration 70c487b9d1299b85ea595a773f3b57d0
“CRANBERRY”Rubber Dam and Accessories（Non-Sterile）
TW: “克朗貝里”橡皮障及其附件（未滅菌）
Taiwan·Risk Class 1·MD·CRANBERRY (M) SDN. BHD.·Registered Oct 01, 2021 – Oct 31, 2026ActiveRegistration details
- Analysis ID
- 70c487b9d1299b85ea595a773f3b57d0
- License Form
- Ministry of Health Medical Device Import Registration No. 009704
- Customs Code
- DHA08400970406
Company information
- Manufacturer
- CRANBERRY (M) SDN. BHD.
- Manufacturer Country
- Malaysia
- Authorized Representative
- SHI SEI INTERNATIONAL LIMITED
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Rubber Dam and Its Accessories (F.6300)".
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F6300 rubber dam and its accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
About this record
Access comprehensive regulatory information for “CRANBERRY”Rubber Dam and Accessories（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 70c487b9d1299b85ea595a773f3b57d0 and manufactured by CRANBERRY (M) SDN. BHD.. The authorized representative in Taiwan is SHI SEI INTERNATIONAL LIMITED.
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