Taiwan FDA registration 9df9eead32bec3eb27fc64f21819b03a

"EMED" Manual gastroenterology-urology surgical instrument and accessories (Non-Sterile)

TW: "醫美德" 手動式胃腸科-泌尿科手術器械及其附件 (未滅菌)

Taiwan·Risk Class 1·MD·EMED SP. ZO.O. SP. K.·Registered Jun 17, 2015 – Jun 17, 2025Expired

Registration details

Analysis ID: 9df9eead32bec3eb27fc64f21819b03a
License Form: Ministry of Health Medical Device Import No. 015352
Customs Code: DHA09401535209

Company information

Manufacturer: EMED SP. ZO.O. SP. K.
Manufacturer Country: Poland
Authorized Representative: REVO LASER CORPORATION

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Gastroenterology-Urology Surgical Instruments and Their Accessories (H.4730)".
Product Type (Level 1): H Gastroenterology-urology devices
Product Type (Level 2): H4730 Manual gastroenterology-urological surgical instruments and accessories
Import Information: Imported from abroad

Dates and status

Registration Date: Jun 17, 2015
Expiry Date: Jun 17, 2025

About this record

Access comprehensive regulatory information for "EMED" Manual gastroenterology-urology surgical instrument and accessories (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 9df9eead32bec3eb27fc64f21819b03a and manufactured by EMED SP. ZO.O. SP. K.. The authorized representative in Taiwan is REVO LASER CORPORATION.

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