Taiwan FDA registration b0d4472fd47a3361bca32221e0f19a85

"Shuyikang" medical gauze (sterilized)

TW: “舒怡康”醫用紗布 (滅菌)

Taiwan·Risk Class 1·HOSPITECH MANUFACTURING SERVICES SDN. BHD.·Registered Aug 14, 2007 – Aug 14, 2022Cancelled

Registration details

Analysis ID: b0d4472fd47a3361bca32221e0f19a85
Customs Code: DHA04400608403

Company information

Manufacturer: HOSPITECH MANUFACTURING SERVICES SDN. BHD.
Manufacturer Country: Malaysia
Authorized Representative: TEAM POWER MEDICAL INSTRUMENT LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Medical Absorbent Fiber (J.5300)".
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.5300 醫療用吸收纖維
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: Aug 14, 2007
Expiry Date: Aug 14, 2022
Cancellation Date: Apr 12, 2024

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Shuyikang" medical gauze (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b0d4472fd47a3361bca32221e0f19a85 and manufactured by HOSPITECH MANUFACTURING SERVICES SDN. BHD.. The authorized representative in Taiwan is TEAM POWER MEDICAL INSTRUMENT LTD..

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.