Taiwan FDA registration c13fac39c7c7eb944dc0f0ac80aecec7

Pentax endoscope attachment (unsterilized)

TW: "賓得"內視鏡附件(未滅菌)

Taiwan·Risk Class 1·HOYA CORPORATION PENTAX MIYAGI FACTORY·Registered Jun 26, 2015 – Jun 26, 2025Expired

Registration details

Analysis ID: c13fac39c7c7eb944dc0f0ac80aecec7
Customs Code: DHA09401539004

Company information

Manufacturer: HOYA CORPORATION PENTAX MIYAGI FACTORY
Manufacturer Country: Japan
Authorized Representative: PENTAX MEDICAL SINGAPORE PTE. LTD. TAIWAN BRANCH(SINGAPORE)

Product details

Intended Use: Limited to the first level recognition range of the "endoscope and its accessories (H.1500)" of the Measures for the Classification and Grading Management of Medical Equipment.
Product Type (Level 1): H Gastroenterology and urology
Product Type (Level 2): H.1500 Internal Scope and its accessories
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: Jun 26, 2015
Expiry Date: Jun 26, 2025

About this record

Access comprehensive regulatory information for Pentax endoscope attachment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c13fac39c7c7eb944dc0f0ac80aecec7 and manufactured by HOYA CORPORATION PENTAX MIYAGI FACTORY. The authorized representative in Taiwan is PENTAX MEDICAL SINGAPORE PTE. LTD. TAIWAN BRANCH(SINGAPORE).

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