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"SHI SEI" Fiber Post (Non-Sterile) - Taiwan Registration 51b32c6d650926a3883942346ff4563a

Access comprehensive regulatory information for "SHI SEI" Fiber Post (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 51b32c6d650926a3883942346ff4563a and manufactured by E. HAHNENKRATT GMBH. The authorized representative in Taiwan is SHI SEI INTERNATIONAL LIMITED.

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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51b32c6d650926a3883942346ff4563a
Registration Details
Taiwan FDA Registration: 51b32c6d650926a3883942346ff4563a
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Device Details

"SHI SEI" Fiber Post (Non-Sterile)
TW: "่ณ‡็”Ÿ" ็Žป็’ƒ็บ–็ถญ็‰™ๆ นๆŸฑ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

51b32c6d650926a3883942346ff4563a

Ministry of Health Medical Device Import No. 014723

DHA09401472300

Company Information

Germany

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Root Canal Center Column Nail (F.3810)".

F Dental devices

F3810 tube center column nail

Imported from abroad

Dates and Status

Dec 05, 2014

Dec 05, 2024