Taiwan FDA registration d28c39d45d2ff2111d2831288080dd39

Photogram light source and its accessories (unsterilized)

TW: "攝譜樂"光源及其附件 (未滅菌)

Taiwan·Risk Class 1·PUFF·Registered Apr 26, 2006 – Apr 26, 2016Cancelled

Registration details

Analysis ID: d28c39d45d2ff2111d2831288080dd39
Customs Code: DHA04400422600

Company information

Manufacturer: PUFF
Manufacturer Country: France
Authorized Representative: ANGEL MEDICAL INSTRUMENT 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: Apr 26, 2006
Expiry Date: Apr 26, 2016
Cancellation Date: Jun 25, 2018

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for Photogram light source and its 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 d28c39d45d2ff2111d2831288080dd39 and manufactured by PUFF. The authorized representative in Taiwan is ANGEL MEDICAL INSTRUMENT 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.