Taiwan FDA registration a231c0a3a28a7be7a7a5de29e44e9f95

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

TW: "史賓格席斯" 耳鼻喉手動式外科器械 (未滅菌)

Taiwan·Risk Class 1·MD·SPIGGLE & THEIS MEDIZINTECHNIK GMBH·Registered Jul 26, 2016 – Jul 26, 2026Expired

Registration details

Analysis ID: a231c0a3a28a7be7a7a5de29e44e9f95
License Form: Ministry of Health Medical Device Import No. 016827
Customs Code: DHA09401682709

Company information

Manufacturer: SPIGGLE & THEIS MEDIZINTECHNIK GMBH
Manufacturer Country: Germany
Authorized Representative: GOLDENSPRING MEDI-TECH CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Manual Surgical Instruments (G.4420)".
Product Type (Level 1): G ENT device
Product Type (Level 2): G4420 OTOLARYNGARY Manual Surgical Instrument
Import Information: Imported from abroad

Dates and status

Registration Date: Jul 26, 2016
Expiry Date: Jul 26, 2026

About this record

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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