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"Herdegen France" Flotation Cushion (Non-Sterile) - Taiwan Registration 70ca0b999897603e3a729e77fa9e7684

Access comprehensive regulatory information for "Herdegen France" Flotation 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 70ca0b999897603e3a729e77fa9e7684 and manufactured by HERDEGEN SAS. The authorized representative in Taiwan is MEDEPOT 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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70ca0b999897603e3a729e77fa9e7684
Registration Details
Taiwan FDA Registration: 70ca0b999897603e3a729e77fa9e7684
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Device Details

"Herdegen France" Flotation Cushion (Non-Sterile)
TW: "ๆณ•ๅœ‹่ท่ฟชๆ น" ๆตฎๅ‹•ๅๅขŠ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

70ca0b999897603e3a729e77fa9e7684

Ministry of Health Medical Device Import No. 020478

DHA09402047802

Company Information

France

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Floating Cushion (O.3175)".

o Equipment for physical medicine

O3175 floating seat cushion

Imported from abroad

Dates and Status

May 23, 2019

May 23, 2024