Vietnam MOH registration 240000459/PCBB-HCM
E.R.C.P. Guiding Tube
VN: Ống thông E.R.C.P
Vietnam·Risk Class TTBYT Loại B·E.R.C.P Catheter·Medi-Globe GmbH·Registered Mar 04, 2024Registration details
- Analysis ID
- 240000459/PCBB-HCM
- Submission ID
- 000.00.19.H29-240228-0010
- Product Type
- E.R.C.P Catheter
- Product Code
- GER-01-18-035, GER-02-18-035, GER-03-18-021, GER-04-18-035, GER-05-18-035, GER-07-18-035, GER-42-25-035
Company information
- Manufacturer
- Medi-Globe GmbH
- Product Owner
- Medi-Globe GmbH
- Authorized Representative
- CÔNG TY TNHH KỸ THUẬT ĐỒNG MINH
Technical details
- Intended Use
- The E.R.C.P. catheter is used to dilate the bile duct and inject the contrast medium.
Dates and status
- Registration Date
- Mar 04, 2024
About this record
Access comprehensive regulatory information for E.R.C.P. Guiding Tube 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 240000459/PCBB-HCM and manufactured by Medi-Globe GmbH. The authorized representative in Vietnam is CÔNG TY TNHH KỸ THUẬT ĐỒNG MINH.
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