Taiwan FDA registration 3a012e3cf6c49f8bfed02b843fbaa207
"Van Strontium Kekel" Skin Pressure Protector (Unsterilized)
TW: "凡鍶克凱爾" 皮膚壓力保護器 (未滅菌)
Taiwan·Risk Class 1·VASCOCARE MEDICAL LTD·Registered Oct 01, 2021 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- 3a012e3cf6c49f8bfed02b843fbaa207
- Customs Code
- DHA08401326801
Company information
- Manufacturer
- VASCOCARE MEDICAL LTD
- Manufacturer Country
- Ireland
- Authorized Representative
- GRAND MEDICAL INSTRUMENT CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of the classification and grading management method of medical equipment, skin pressure protector (J.6450).
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6450 Skin Pressure Protector
- Import Information
- import
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for "Van Strontium Kekel" Skin Pressure Protector (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3a012e3cf6c49f8bfed02b843fbaa207 and manufactured by VASCOCARE MEDICAL LTD. The authorized representative in Taiwan is GRAND MEDICAL INSTRUMENT CO., LTD..
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