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HSA · registration DE0509268

Pulmodyne GO-PAP

SingaporeAnaesthesiologyClass BPulmodyne, Inc.
Official record identity
Registration number
DE0509268
Model name
Neb-Connect; GO-PAP, 5.0/7.5/10.0cm PEEP Levels, BiTrac ED Mask (Adult Small); GO-PAP with Included Nebulizer, 5.0/7.5/10.0cm PEEP Levels, BiTrac ED Mask (Adult Small); GO-PAP, 5.0/7.5/10.0cm PEEP Levels, BiTrac ED Mask (Adult Medium); GO-PAP with Included Nebulizer, 5.0/7.5/10.0cm PEEP Levels, BiTrac ED Mask (Adult Medium); GO-PAP plus Neb-Connect, with Included Nebulizer, 5.0/7.5/10.0cm PEEP Levels, BiTrac ED Mask (Adult Medium); GO-PAP, 5.0/7.5/10.0cm PEEP Levels, BiTrac ED Mask (Adult Large); GO-PAP with Included Nebulizer, 5.0/7.5/10.0cm PEEP Levels, BiTrac ED Mask (Adult Large); GO-PAP plus Neb-Connect, with Included Nebulizer, 5.0/7.5/10.0cm PEEP Levels, BiTrac ED Mask (Adult Large); GO-PAP, 5.0/7.5/10.0cm PEEP Levels, BiTrac ED Mask (Adult Medium); GO-PAP with Included Nebulizer, 5.0/7.5/10.0cm PEEP Levels, BiTrac ED Mask (Adult Medium); GO-PAP plus Neb-Connect, with Included Nebulizer, 5.0/7.5/10.0cm PEEP Levels, BiTrac ED Mask (Adult Medium); GO-PAP, 5.0/7.5/10.0cm PEEP Levels, BiTrac ED Mask (Adult Large); GO-PAP with Included Nebulizer, 5.0/7.5/10.0cm PEEP Levels, BiTrac ED Mask (Adult Large); GO-PAP plus Neb-Connect, with Included Nebulizer, 5.0/7.5/10.0cm PEEP Levels, BiTrac ED Mask (Adult Large)
Model identifier
313-011111; 313-4601; 313-4601N; 313-4602; 313-4602N; 313-4602NC; 313-4603; 313-4603N; 313-4603NC; 313-4604; 313-4604N; 313-4604NC; 313-4605; 313-4605N; 313-4605NC
Registration date
May 08, 2024
Classification
Risk class
Class B
Official value: CLASS B
Published category
Anaesthesiology
Published parties
Product owner
Pulmodyne, Inc.
Registrant / registration holder
I:EMEDICS PTE. LTD.
Official description

Pulmodyne’s Go-PAP delivers continuous positive airway pressure (CPAP) throughout the breathing cycle. It provides CPAP at preset levels throughout inspiration and exhalation, independent of the patient’s flow rate. Go-PAP system is intended for use on spontaneously breathing patients.

Additional source fields
Product owner address
2055 Executive Dr, Indianapolis, IN 46241, Indiana, United States
Registrant address
31 KAKI BUKIT ROAD 3, #05-12, TECHLINK, Singapore 417818
About this record

This page mirrors one row from HSA’s official registered-medical-device workbook. Product owner and registrant are separate published roles; neither is relabeled as the manufacturer. The official NOT_GENERATED value is retained when HSA does not publish a registration number, and the device name remains part of the stable record identity.