Taiwan FDA registration ab0da1603b35dcca95c98e91fda7b88b

"Guise" ENT Manual Surgical Instruments (Unsterilized)

TW: “吉斯”耳鼻喉手動式外科器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·GYRUS MEDICAL GMBH·Registered Jul 06, 2007 – Jul 06, 2017Cancelled
Registration details
Analysis ID
ab0da1603b35dcca95c98e91fda7b88b
Customs Code
DHA04400599003
Company information
Manufacturer
GYRUS MEDICAL GMBH
Manufacturer Country
Germany
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Manual Surgical Instruments (G.4420)".
Product Type (Level 1)
G ENT Science
Product Type (Level 2)
G.4420 Otolaryngology manual surgical instruments
Import Information
import
Dates and status
Registration Date
Jul 06, 2007
Expiry Date
Jul 06, 2017
Cancellation Date
Nov 20, 2019
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "Guise" ENT Manual Surgical Instruments (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ab0da1603b35dcca95c98e91fda7b88b and manufactured by GYRUS MEDICAL GMBH. The authorized representative in Taiwan is MEDFRONT MEDICAL TECHNOLOGY CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including GYRUS ENT LLC, and 1 recent registrations in the same category. 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.

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