Taiwan FDA registration 94a5e2886ec0482a3e6f46e7d0fab56a
“NAR” ARS Decompression Needle (Sterile)
TW: “納爾” 艾爾斯解壓針(滅菌)
Taiwan·Risk Class 2·MD·NORTH AMERICAN RESCUE, LLC·Registered Jun 08, 2023 – Jun 08, 2028ActiveRegistration details
- Analysis ID
- 94a5e2886ec0482a3e6f46e7d0fab56a
- License Form
- Ministry of Health Medical Device Import No. 036374
- Customs Code
- DHA05603637403
Company information
- Manufacturer
- NORTH AMERICAN RESCUE, LLC
- Manufacturer Country
- United States
- Authorized Representative
- CORELEADER BIOTECH CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E1300 catheter cannula
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 08, 2023
- Expiry Date
- Jun 08, 2028
About this record
Access comprehensive regulatory information for “NAR” ARS Decompression Needle (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 94a5e2886ec0482a3e6f46e7d0fab56a and manufactured by NORTH AMERICAN RESCUE, LLC. The authorized representative in Taiwan is CORELEADER BIOTECH CO., LTD..
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