Taiwan FDA registration 530797343b12ba132e163cc38afa352c

Manual orthopedic instruments "Le Del" (unsterilized)

TW: “樂得爾”手動式骨科手術器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·LDR MEDICAL·Registered Sep 02, 2009 – Sep 02, 2014Cancelled
Registration details
Analysis ID
530797343b12ba132e163cc38afa352c
Customs Code
DHA04400802803
Company information
Manufacturer
LDR MEDICAL
Manufacturer Country
France
Authorized Representative
HOLLING BIO-PHARMA. CORP.
Product details
Intended Use
Limited to the first level identification range of manual orthopedic surgical instruments (N.4540) of the Measures for the Administration of Medical Equipment.
Product Type (Level 1)
N Orthopedics
Product Type (Level 2)
N.4540 手動式骨科手術器械
Import Information
import
Dates and status
Registration Date
Sep 02, 2009
Expiry Date
Sep 02, 2014
Cancellation Date
Aug 09, 2018
Cancellation information
Status
Logged out
Reason
未展延而逾期者
About this record

Access comprehensive regulatory information for Manual orthopedic instruments "Le Del" (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 530797343b12ba132e163cc38afa352c and manufactured by LDR MEDICAL. The authorized representative in Taiwan is HOLLING BIO-PHARMA. CORP..

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