Taiwan FDA registration 386ec8032ec91dce5abbdbabd8f171e2

"Hanz" flexible laryngoscope (unsterilized)

TW: “漢茲”可彎曲式喉頭鏡 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·KARLHEINZ HINZE OPTOENGINEERING GMBH&CO·Registered Apr 11, 2007 – Apr 11, 2012Cancelled
Registration details
Analysis ID
386ec8032ec91dce5abbdbabd8f171e2
Customs Code
DHA04400573806
Company information
Manufacturer Country
Germany
Authorized Representative
MEDWAY BME CORPORATION
Product details
Intended Use
Limited to the first level of identification range of "Flexible Laryngoscope (D.5530)" under the Measures for the Administration of Medical Devices.
Product Type (Level 1)
D Anesthesiology
Product Type (Level 2)
D.5530 Curved laryngeal lenses
Import Information
import
Dates and status
Registration Date
Apr 11, 2007
Expiry Date
Apr 11, 2012
Cancellation Date
Apr 30, 2014
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "Hanz" flexible laryngoscope (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 386ec8032ec91dce5abbdbabd8f171e2 and manufactured by KARLHEINZ HINZE OPTOENGINEERING GMBH&CO. The authorized representative in Taiwan is MEDWAY BME CORPORATION.

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.

Free DatabasePowered by Pure Global AI89,000+ Devices