Taiwan FDA registration c23ef2c1334567ac230a57802a58ceed
“Geister” CleanLoop Sterilization Container
TW: “杰士特”科林樂普滅菌盒
Taiwan·Risk Class 2·MD·GEISTER MEDIZINTECHNIK GMBH·Registered Dec 05, 2018 – Dec 05, 2023ExpiredRegistration details
- Analysis ID
- c23ef2c1334567ac230a57802a58ceed
- License Form
- Ministry of Health Medical Device Import No. 031899
- Customs Code
- DHA05603189901
Company information
- Manufacturer
- GEISTER MEDIZINTECHNIK GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- PLOVER MEDICAL INSTRUMENTS, INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J6850 sterilization kit
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 05, 2018
- Expiry Date
- Dec 05, 2023
About this record
Access comprehensive regulatory information for “Geister” CleanLoop Sterilization Container in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c23ef2c1334567ac230a57802a58ceed and manufactured by GEISTER MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is PLOVER MEDICAL INSTRUMENTS, INC..
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