Taiwan FDA registration 66e878a34b90d9081483c833d390fd3e

“Geister” SURGIMOTOR Sternum Saws (Non-Sterile)

TW: “杰士特”手術用胸骨鋸(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·GEISTER MEDIZINTECHNIK GMBH·Registered Jan 18, 2019 – Jan 18, 2024Expired
Registration details
Analysis ID
66e878a34b90d9081483c833d390fd3e
License Form
Ministry of Health Medical Device Import No. 020039
Customs Code
DHA09402003902
Company information
Manufacturer Country
Germany
Authorized Representative
PLOVER MEDICAL INSTRUMENTS, INC.
Product details
Intended Use
Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Surgical Instruments, Motors and Accessories or Accessories (I.4820)".
Product Type (Level 1)
I General and plastic surgical devices
Product Type (Level 2)
I4820 Surgical Appliance Motors with Accessories or Accessories
Import Information
Imported from abroad
Dates and status
Registration Date
Jan 18, 2019
Expiry Date
Jan 18, 2024
About this record

Access comprehensive regulatory information for “Geister” SURGIMOTOR Sternum Saws (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 66e878a34b90d9081483c833d390fd3e and manufactured by GEISTER MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is PLOVER MEDICAL INSTRUMENTS, 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