Taiwan FDA registration 155af18b5fed9467b3f2a0e5875a0f51

"Flex" non-electric coil blade (unsterilized)

TW: “福萊克斯” 非電力圈刃(未滅菌)

Taiwan·Risk Class 1·ENDO-FLEX GMBH·Registered Jun 28, 2010 – Jun 28, 2025Expired

Registration details

Analysis ID: 155af18b5fed9467b3f2a0e5875a0f51
Customs Code: DHA04400894105

Company information

Manufacturer: ENDO-FLEX GMBH
Manufacturer Country: Germany
Authorized Representative: IDS MEDICAL SYSTEMS (HONG KONG) COMPANY LIMITED, TAIWAN BRANCH (HONG KONG)

Product details

Intended Use: Limited to the first level identification scope of the classification and grading management method for medical equipment "Manual Gastroenterology-Urology Surgical Instruments and Their Accessories (H.4730)".
Product Type (Level 1): H Gastroenterology and urology
Product Type (Level 2): H.4730 H.4730 Hand Gastroentero-Urology Surgical Instruments and Accessories
Import Information: import

Dates and status

Registration Date: Jun 28, 2010
Expiry Date: Jun 28, 2025

About this record

Access comprehensive regulatory information for "Flex" non-electric coil blade (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 155af18b5fed9467b3f2a0e5875a0f51 and manufactured by ENDO-FLEX GMBH. The authorized representative in Taiwan is IDS MEDICAL SYSTEMS (HONG KONG) COMPANY LIMITED, TAIWAN BRANCH (HONG KONG).

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