Taiwan FDA registration 3aa3b48a5420a1fcdc0d6cc9d4566c0f
"Iolo" blood lancet needle
TW: "愛奧樂" 採血針
Taiwan·Risk Class 1·SUSHOU SPR MEDICAL DEVICES DEVELOPMENT CO., LTD.·Registered Nov 26, 2008 – Nov 26, 2013CancelledRegistration details
- Analysis ID
- 3aa3b48a5420a1fcdc0d6cc9d4566c0f
- Customs Code
- DHA04600059501
Company information
- Manufacturer
- SUSHOU SPR MEDICAL DEVICES DEVELOPMENT CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- BIOLAND MEDICAL TECHNOLOGY LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Nov 26, 2008
- Expiry Date
- Nov 26, 2013
- Cancellation Date
- Jun 11, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Iolo" blood lancet needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3aa3b48a5420a1fcdc0d6cc9d4566c0f and manufactured by SUSHOU SPR MEDICAL DEVICES DEVELOPMENT CO., LTD.. The authorized representative in Taiwan is BIOLAND MEDICAL TECHNOLOGY 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