Taiwan FDA registration 11d4d037ef143a75c35e406cd8fcee80

"Herb" manual instruments for general surgery (unsterilized)

TW: "賀伯"一般手術用手動式器械(未滅菌)

Taiwan·Risk Class 1·HEBU MEDICAL GMBH·Registered Jun 02, 2011 – Jun 02, 2021Cancelled

Registration details

Analysis ID: 11d4d037ef143a75c35e406cd8fcee80
Customs Code: DHA04401043600

Company information

Manufacturer: HEBU MEDICAL GMBH
Manufacturer Country: Germany
Authorized Representative: BIOLAND ENTERPRISE INC.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4800 Hand Instruments for General Surgery
Import Information: import

Dates and status

Registration Date: Jun 02, 2011
Expiry Date: Jun 02, 2021
Cancellation Date: Oct 12, 2023

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for "Herb" manual instruments for general surgery (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 11d4d037ef143a75c35e406cd8fcee80 and manufactured by HEBU MEDICAL GMBH. The authorized representative in Taiwan is BIOLAND ENTERPRISE INC..

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.