Taiwan FDA registration 90cb1a489034f11e4f74eed02009e567

"Holy Light" Skin Pressure Protector (Non-Sterilized)

TW: "聖光" 皮膚壓力保護器 (未滅菌)

Taiwan·Risk Class 1·Sungkwang Meditech Co., Ltd.·Registered Oct 25, 2024 – Oct 31, 2025Expired

Registration details

Analysis ID: 90cb1a489034f11e4f74eed02009e567
Customs Code: DHA084A0031407

Company information

Manufacturer: Sungkwang Meditech Co., Ltd.
Manufacturer Country: Korea, Republic of
Authorized Representative: HONG SHENG MEDICAL INSTRUMENTS CO.

Product details

Intended Use: Limited to the first level identification scope of the skin pressure protector (J.6450) for the classification and grading management of medical devices.
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 25, 2024
Expiry Date: Oct 31, 2025

About this record

Access comprehensive regulatory information for "Holy Light" Skin Pressure Protector (Non-Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 90cb1a489034f11e4f74eed02009e567 and manufactured by Sungkwang Meditech Co., Ltd.. The authorized representative in Taiwan is HONG SHENG MEDICAL INSTRUMENTS CO..

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.