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"Van Strontium Kekel" Skin Pressure Protector (Unsterilized) - Taiwan Registration 3a012e3cf6c49f8bfed02b843fbaa207

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..

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.

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3a012e3cf6c49f8bfed02b843fbaa207
Registration Details
Taiwan FDA Registration: 3a012e3cf6c49f8bfed02b843fbaa207
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Device Details

"Van Strontium Kekel" Skin Pressure Protector (Unsterilized)
TW: "ๅ‡ก้ถๅ…‹ๅ‡ฑ็ˆพ" ็šฎ่†šๅฃ“ๅŠ›ไฟ่ญทๅ™จ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

3a012e3cf6c49f8bfed02b843fbaa207

DHA08401326801

Company Information

Ireland

Product Details

Limited to the first level recognition range of the classification and grading management method of medical equipment, skin pressure protector (J.6450).

J General hospital and personal use equipment

J.6450 Skin Pressure Protector

import

Dates and Status

Oct 01, 2021

Oct 31, 2025