Vietnam MOH registration 240001411/PCBB-HCM
One-time use ureteral stent
VN: Giá đỡ niệu quản dùng một lần
Registration details
- Analysis ID
- 240001411/PCBB-HCM
- Submission ID
- 000.00.19.H29-240619-0008
- Product Type
- 980-10-35, 980-10-45, 980-11-35, 980-11-45, 980-12-35, 980-12-40, 980-12-45, 980-13-35, 980-13-45, 980-14-16, 980-14-35, 980-14-45
Company information
- Manufacturer
- Nanchang Woek Medical Technology Co., Ltd
- Product Owner
- Nanchang Woek Medical Technology Co., Ltd
- Authorized Representative
- CÔNG TY TNHH WELL LEAD MEDICAL VIỆT NAM
Technical details
- Intended Use
- Used to establish a channel for instruments such as the endoscope to enter the urinary tract during urological surgery. The Y-shaped design has a side tube to connect to the negative pressure suction device, improving visualization and endoscopic procedures
Dates and status
- Registration Date
- Jul 08, 2024
About this record
Access comprehensive regulatory information for One-time use ureteral stent in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TTBYT Loại B medical device is registered under number 240001411/PCBB-HCM and manufactured by Nanchang Woek Medical Technology Co., Ltd. The authorized representative in Vietnam is CÔNG TY TNHH WELL LEAD MEDICAL VIỆT NAM.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 300,000+ Vietnamese medical device registrations, helping global MedTech companies navigate Vietnam MOH regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI300,000+ Devices