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E.R.C.P. Guiding Tube - Vietnam Registration 240000459/PCBB-HCM

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 Loแบกi B medical device is registered under number 240000459/PCBB-HCM and manufactured by Medi-Globe GmbH. The authorized representative in Vietnam is Cร”NG TY TNHH KYฬƒ THUร‚ฬฃT ฤร”ฬ€NG 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.

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240000459/PCBB-HCM
Registration Details
Vietnam MOH Registration: 240000459/PCBB-HCM
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Device Details

E.R.C.P. Guiding Tube
VN: แปng thรดng E.R.C.P
Risk Class TTBYT Loแบกi B

Registration Details

240000459/PCBB-HCM

000.00.19.H29-240228-0010

E.R.C.P Catheter

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

Medi-Globe GmbH

Technical Details

The E.R.C.P. catheter is used to dilate the bile duct and inject the contrast medium.

Dates and Status

Mar 04, 2024