Taiwan FDA registration d4cfc629063c421595be950fdc394055
"Cleo Selebi" Ayo rectal dilator (unsterilized)
TW: “克里歐世勒比”愛優直腸擴張器（未滅菌）
Taiwan·Risk Class 1·CRYOTHERAPY PAIN RELIEF PRODUCTS INC·Registered Apr 02, 2009 – Apr 02, 2014CancelledRegistration details
- Analysis ID
- d4cfc629063c421595be950fdc394055
- Customs Code
- DHA04400761602
Company information
- Manufacturer
- CRYOTHERAPY PAIN RELIEF PRODUCTS INC
- Manufacturer Country
- United States
- Authorized Representative
- MEDLION BIOTECH CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of "rectal dilator (H.5450)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5450 Rectal dilator
- Import Information
- import
Dates and status
- Registration Date
- Apr 02, 2009
- Expiry Date
- Apr 02, 2014
- Cancellation Date
- Dec 14, 2016
Cancellation information
- Status
- Logged out
- Reason
- 屆期未申請展延
About this record
Access comprehensive regulatory information for "Cleo Selebi" Ayo rectal dilator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d4cfc629063c421595be950fdc394055 and manufactured by CRYOTHERAPY PAIN RELIEF PRODUCTS INC. The authorized representative in Taiwan is MEDLION BIOTECH CO., LTD..
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