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"Spiggle & Theis" Ear, nose and throat manual surgical instrument (Non-Sterile) - Taiwan Registration a231c0a3a28a7be7a7a5de29e44e9f95

Access comprehensive regulatory information for "Spiggle & Theis" Ear, nose and throat manual surgical instrument (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 a231c0a3a28a7be7a7a5de29e44e9f95 and manufactured by SPIGGLE & THEIS MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is GOLDENSPRING MEDI-TECH CO., LTD..

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a231c0a3a28a7be7a7a5de29e44e9f95
Registration Details
Taiwan FDA Registration: a231c0a3a28a7be7a7a5de29e44e9f95
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Device Details

"Spiggle & Theis" Ear, nose and throat manual surgical instrument (Non-Sterile)
TW: "ๅฒ่ณ“ๆ ผๅธญๆ–ฏ" ่€ณ้ผปๅ–‰ๆ‰‹ๅ‹•ๅผๅค–็ง‘ๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

a231c0a3a28a7be7a7a5de29e44e9f95

Ministry of Health Medical Device Import No. 016827

DHA09401682709

Company Information

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Manual Surgical Instruments (G.4420)".

G ENT device

G4420 OTOLARYNGARY Manual Surgical Instrument

Imported from abroad

Dates and Status

Jul 26, 2016

Jul 26, 2026