Taiwan FDA registration f56614b96716746545ffa600fce455de
"Heavy Surplus" Wound Care Kit (Sterilized)
TW: "重餘" 傷口護理包 (滅菌)
Registration details
- Analysis ID
- f56614b96716746545ffa600fce455de
- Customs Code
- DHA09600248905
Company information
- Manufacturer
- SPRO MEDICAL PRODUCTS (XIAMEN) CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- CHONG YU INTERNATIONAL MARKETING CORPORATION
Product details
- Intended Use
- It is limited to the first-level identification scope of the "Medical Absorbent Fiber (J.5300)" and "General Surgical Manual Instrument (I.4800)" in the Administrative Measures for Classification and Classification of Medical Devices.
- Product Type (Level 1)
- J General hospital and personal use equipment;; I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Manual instruments for general surgery; J.5300 Absorbent fibers for medical use
- Import Information
- QMS/QSD;; Input;; Chinese goods
Dates and status
- Registration Date
- Sep 09, 2015
- Expiry Date
- Sep 09, 2025
About this record
Access comprehensive regulatory information for "Heavy Surplus" Wound Care Kit (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f56614b96716746545ffa600fce455de and manufactured by SPRO MEDICAL PRODUCTS (XIAMEN) CO., LTD.. The authorized representative in Taiwan is CHONG YU INTERNATIONAL MARKETING CORPORATION.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices