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"Ceracarta" Patient Lubricant (Non-sterile) - Taiwan Registration f70da78013b1fdceb399ab36d73a380f

Access comprehensive regulatory information for "Ceracarta" Patient Lubricant (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 f70da78013b1fdceb399ab36d73a380f and manufactured by CERACARTA S.P.A. The authorized representative in Taiwan is PAI LEA ENT. 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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f70da78013b1fdceb399ab36d73a380f
Registration Details
Taiwan FDA Registration: f70da78013b1fdceb399ab36d73a380f
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Device Details

"Ceracarta" Patient Lubricant (Non-sterile)
TW: "ๅ–œๆจ‚้”" ็—…ๆ‚ฃ็”จๆฝคๆป‘ๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

f70da78013b1fdceb399ab36d73a380f

Ministry of Health Medical Device Import No. 015715

DHA09401571506

Company Information

Italy

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Lubricants for Patients (J.6375)".

J General hospital and personal use equipment

J6375 Lubricant for patients

Imported from abroad

Dates and Status

Oct 05, 2015

Oct 05, 2025