Taiwan FDA registration 334fc5dcee19cdc78f3bb664e7b87f5a
“APEX”PRESSURE RELIEF PAD (Non-Sterile)
TW: “雅博”減壓氣墊 (未滅菌)
Taiwan·Risk Class 1·MD·APEX MEDICAL (KUNSHAN) CORP.·Registered Jan 19, 2007 – Jan 19, 2027ActiveRegistration details
- Analysis ID
- 334fc5dcee19cdc78f3bb664e7b87f5a
- License Form
- Department of Health Medical Device Land Transport No. 000338
- Customs Code
- DHA04600033807
Company information
- Manufacturer
- APEX MEDICAL (KUNSHAN) CORP.
- Manufacturer Country
- China
- Authorized Representative
- Wellell Inc.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Alternating Pressure Air Mattress (J.5550)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J5550 Alternating pressure air mattress
- Import Information
- Imported from abroad; Made in China
Dates and status
- Registration Date
- Jan 19, 2007
- Expiry Date
- Jan 19, 2027
About this record
Access comprehensive regulatory information for “APEX”PRESSURE RELIEF PAD (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 334fc5dcee19cdc78f3bb664e7b87f5a and manufactured by APEX MEDICAL (KUNSHAN) CORP.. The authorized representative in Taiwan is Wellell Inc..
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