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"J.P." Cushion (Non-Sterile) - Taiwan Registration 1abc9644d901268b5956546cd70ed8d2

Access comprehensive regulatory information for "J.P." Cushion (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1abc9644d901268b5956546cd70ed8d2 and manufactured by SEALTECH., LTD. The authorized representative in Taiwan is J. P. 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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1abc9644d901268b5956546cd70ed8d2
Registration Details
Taiwan FDA Registration: 1abc9644d901268b5956546cd70ed8d2
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Device Details

"J.P." Cushion (Non-Sterile)
TW: "ๅปบ้ตฌ" ๆตฎๅ‹•ๅๅขŠ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

1abc9644d901268b5956546cd70ed8d2

Ministry of Health Medical Device Import No. 022821

DHA09402282109

Company Information

Korea, Republic of

Product Details

Limited to the first level identification scope of the "floating cushion (O.3175)" of the Measures for the Classification and Grading Management of Medical Equipment.

o Physical Medical Sciences

O3175 floating seat cushion

Imported from abroad

Dates and Status

Jun 06, 2022

Jun 06, 2027