Taiwan FDA registration 45eff3e064cde6f8105ef2f2ec290faf
"Cardino" Venturi mask (unsterilized)
TW: "卡迪諾" Venturi面罩 (未滅菌)
Registration details
- Analysis ID
- 45eff3e064cde6f8105ef2f2ec290faf
- Customs Code
- DHA04400247501
Company information
- Manufacturer
- PRODUCTOS UROLOGOS DE MEXICO, S.A. DE C.V.
- Manufacturer Country
- Mexico
- Authorized Representative
- Mitutoyo Medical Equipment Co., Ltd
Product details
- Intended Use
- The Venturi mask is a device that mixes air and oxygen. 100% oxygen can be diluted to a predetermined concentration and the gas mixture can be infused into the patient.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5600 Venturi面罩
- Import Information
- import
Dates and status
- Registration Date
- Jan 06, 2006
- Expiry Date
- Jan 06, 2011
- Cancellation Date
- Nov 23, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Cardino" Venturi mask (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 45eff3e064cde6f8105ef2f2ec290faf and manufactured by PRODUCTOS UROLOGOS DE MEXICO, S.A. DE C.V.. The authorized representative in Taiwan is Mitutoyo Medical Equipment 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