Taiwan FDA registration 9595bacfdde6cdefb9d088d29948c708

Shakessell blood rate sedimentation test equipment

TW: 莎仕德血液速率沉降測試器材
Taiwan flagTaiwan·Risk Class 1·SARSTEDT AG & CO.·Registered Nov 17, 2005 – Nov 17, 2015Cancelled
Registration details
Analysis ID
9595bacfdde6cdefb9d088d29948c708
Customs Code
DHA04400200602
Company information
Manufacturer
SARSTEDT AG & CO.
Manufacturer Country
Germany
Authorized Representative
PAN ASIA BIOMEDICAL TECHNOLOGY INC.
Product details
Intended Use
測量人體全血中紅血細胞的沉降速率.
Product Type (Level 1)
B Hematology, pathology, and genetics
Product Type (Level 2)
B.6700 紅血球沈澱速率試驗
Import Information
import
Dates and status
Registration Date
Nov 17, 2005
Expiry Date
Nov 17, 2015
Cancellation Date
Aug 14, 2018
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for Shakessell blood rate sedimentation test equipment in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9595bacfdde6cdefb9d088d29948c708 and manufactured by SARSTEDT AG & CO.. The authorized representative in Taiwan is PAN ASIA BIOMEDICAL TECHNOLOGY 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.

Free DatabasePowered by Pure Global AI89,000+ Devices