Vietnam MOH registration 240001440/PCBB-HCM

Endotracheal Tube / Double-lumen Endobronchial Tube

VN: Ống nội phế quản/ Ống nội khí quản 2 nòng

Vietnam·Risk Class TTBYT Loại B·Theo theo phụ lục·ECAN MEDICAL CO., LTD·Registered Jul 09, 2024

Registration details

Analysis ID: 240001440/PCBB-HCM
Submission ID: 000.00.19.H29-240701-0013
Product Type: Theo theo phụ lục
Product Code: Theo phụ lục

Company information

Manufacturer: ECAN MEDICAL CO., LTD
Manufacturer Country: Theo theo phụ lục
Product Owner: ECAN MEDICAL CO., LTD
Authorized Representative: CÔNG TY CỔ PHẦN THƯƠNG MẠI CÔNG NGHỆ TÂM Y

Technical details

Intended Use: It is used in heart surgery or as an anesthetic in lung surgery, and it is also used in selective lung collapse or in cases of severe lung disease in patients with pneumonia, to improve the patient's ability to tolerate surgery and to facilitate the surgical procedure.

Dates and status

Registration Date: Jul 09, 2024

About this record

Access comprehensive regulatory information for Endotracheal Tube / Double-lumen Endobronchial 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 240001440/PCBB-HCM and manufactured by ECAN MEDICAL CO., LTD. The authorized representative in Vietnam is CÔNG TY CỔ PHẦN THƯƠNG MẠI CÔNG NGHỆ TÂM Y.

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.