Taiwan FDA registration fb1f1b86ca51d14c52006548e26dcd09

"Carforson" involves a bone marrow section/tissue extraction needle

TW: "卡弗迅"介入體骨髓切片/組織抽取針
Taiwan flagTaiwan·Risk Class 2·BARD PERIPHERAL VASCULAR, INC.;; CAREFUSION 2200, INC.·Registered Dec 06, 2004 – Dec 06, 2024Expired
Registration details
Analysis ID
fb1f1b86ca51d14c52006548e26dcd09
Customs Code
DHA00601094501
Company information
Manufacturer Country
United States
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order.
Product Type (Level 1)
H Gastroenterology and urology
Import Information
import
Dates and status
Registration Date
Dec 06, 2004
Expiry Date
Dec 06, 2024
About this record

Access comprehensive regulatory information for "Carforson" involves a bone marrow section/tissue extraction needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fb1f1b86ca51d14c52006548e26dcd09 and manufactured by BARD PERIPHERAL VASCULAR, INC.;; CAREFUSION 2200, INC.. The authorized representative in Taiwan is BECTON DICKINSON HOLDINGS PTE. LTD. TAIWAN BRANCH (SINGAPORE).

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