Taiwan FDA registration 92e54afd21867ee7fe471793f8ccbcf1
"Hao Shi Bi & Hao Kaier" Meidi oxygen nasal cannula
TW: "郝士比&郝愷爾" 美迪氧氣鼻管
Taiwan·Risk Class 1·HOSPITAL & HOMECARE MEDICAL DEVICE CO., LTD. YANGZHONG·Registered Dec 02, 2005 – Dec 02, 2010CancelledRegistration details
- Analysis ID
- 92e54afd21867ee7fe471793f8ccbcf1
- Customs Code
- DHA04600007208
Company information
- Manufacturer Country
- China
- Authorized Representative
- DURAMED INTERNATIONAL CORPORATION
Product details
- Intended Use
- A device with two protrusions that can inject oxygen through the patient's nostrils.
- Product Type (Level 1)
- D Anesthesiology
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Dec 02, 2005
- Expiry Date
- Dec 02, 2010
- Cancellation Date
- Apr 20, 2011
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Hao Shi Bi & Hao Kaier" Meidi oxygen nasal cannula in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 92e54afd21867ee7fe471793f8ccbcf1 and manufactured by HOSPITAL & HOMECARE MEDICAL DEVICE CO., LTD. YANGZHONG. The authorized representative in Taiwan is DURAMED INTERNATIONAL CORPORATION.
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