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Electric Intensive Care Bed and Accessories - Vietnam Registration 240000820/PCBB-HN

Access comprehensive regulatory information for Electric Intensive Care Bed and Accessories 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 240000820/PCBB-HN and manufactured by HILL-ROM, INC. The authorized representative in Vietnam is VĂN PHÒNG ĐẠI DIỆN BAXTER HEALTHCARE (ASIA) PTE LTD TẠI THÀNH PHỐ HÀ NỘI.

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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240000820/PCBB-HN
Registration Details
Vietnam MOH Registration: 240000820/PCBB-HN
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Device Details

Electric Intensive Care Bed and Accessories
VN: Giường hồi sức cấp cứu điều khiển điện và phụ kiện
Risk Class TTBYT Loại B

Registration Details

240000820/PCBB-HN

000.00.19.H26-240320-0001

Theo theo phụ lục

Theo phụ lục

Company Information

Theo theo phụ lục

HILL-ROM, INC

Technical Details

The Progressa Bed is designed for use in the treatment or prevention of pulmonary complications or other complications related to immobility; for the treatment or prevention of pressure ulcers; or in any other case where medical benefit can be derived from Continuous Lateral Rotation Therapy or Percussive/Rhythmic Therapy. The Progressa Bed is designed to support patients in a medical environment. The Progressa Bed can be used in a variety of settings, including but not limited to, acute care, including intensive care, de-escalation/escalation care, medical/surgical, less acute care, and the Post-Anesthesia Care Unit (PACU) and various departments of the Emergency Department (ED). The Progressa Bed can be used for a diverse range of patient types if deemed appropriate by the medical staff or the medical facility. The intended users of this product are trained medical personnel who are capable of operating and controlling the product and who have the physical and cognitive abilities to do so safely. There are certain features and controls on the bed that can be used by patients and their families, but only under the proper guidance of medical personnel. If the patient does not have the physical strength or cognitive abilities to operate and control the product safely, the medical facility's safety protocols should be followed.

Dates and Status

Apr 19, 2024