Taiwan FDA registration f20e8bd8c7f8f4821c960722b59a0a7e

"Wishapp" ENT Lighting Fiber Optic Light Source and Accessories (Unsterilized)

TW: “威夏普”耳鼻喉照明光纖光源及配件 (未滅菌)

Taiwan·Risk Class 1·WISAP MEDICAL TECHNOLOGY GMBH·Registered Oct 27, 2006 – Oct 27, 2016Cancelled

Registration details

Analysis ID: f20e8bd8c7f8f4821c960722b59a0a7e
Customs Code: DHA04400527202

Company information

Manufacturer: WISAP MEDICAL TECHNOLOGY GMBH
Manufacturer Country: Germany
Authorized Representative: BEAMED INSTRUMENTS CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Fiber Optic Light Source and Vehicle (G.4350)".
Product Type (Level 1): G ENT Science
Product Type (Level 2): G.4350 Ear, nose and throat optical fiber light sources and carriers
Import Information: import

Dates and status

Registration Date: Oct 27, 2006
Expiry Date: Oct 27, 2016
Cancellation Date: Dec 22, 2016

Cancellation information

Status: Logged out
Reason: 自請註銷

About this record

Access comprehensive regulatory information for "Wishapp" ENT Lighting Fiber Optic Light Source and Accessories (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f20e8bd8c7f8f4821c960722b59a0a7e and manufactured by WISAP MEDICAL TECHNOLOGY GMBH. The authorized representative in Taiwan is BEAMED INSTRUMENTS CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.