Taiwan FDA registration b075cb12fa4353756d69a3d27ce392ec

"Yeka" manual stethoscope (unsterilized)

TW: “耶卡”手動聽診器（未滅菌）

Taiwan·Risk Class 1·ERKA. KALLMEYER MEDIZINTECHNIK GMBH & CO. KG·Registered Dec 28, 2009 – Dec 28, 2024Expired

Registration details

Analysis ID: b075cb12fa4353756d69a3d27ce392ec
Customs Code: DHA04400842401

Company information

Manufacturer: ERKA. KALLMEYER MEDIZINTECHNIK GMBH & CO. KG
Manufacturer Country: Germany
Authorized Representative: MEDIBIOT CO., LTD.

Product details

Intended Use: Limited to the first level of identification scope of the "Stethoscope (E.1875)" of the Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): E Cardiovascular Medicine Science
Product Type (Level 2): E.1875 Listening device
Import Information: import

Dates and status

Registration Date: Dec 28, 2009
Expiry Date: Dec 28, 2024

About this record

Access comprehensive regulatory information for "Yeka" manual stethoscope (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b075cb12fa4353756d69a3d27ce392ec and manufactured by ERKA. KALLMEYER MEDIZINTECHNIK GMBH & CO. KG. The authorized representative in Taiwan is MEDIBIOT CO., LTD..

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