Consulting Wallah › Device Explorer › Other devices › Chest-oscillation airway secretion-clearing system
Device Explorer · FDA GUDID · GMDN 38124

Chest-oscillation airway secretion-clearing system

An assembly of devices designed to provide high frequency chest wall oscillation (HFCWO) for external chest wall manipulation intended to loosen excessive airway secretions [mucus or sputum (phlegm)] to promote airway clearance and improve bronchial drainage f

US‑registered devices130in commercial distribution
Companies3labelers on GUDID
Single‑use24%of device records
Sterile0%labelled sterile
Prescription6%Rx‑only share
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Share of device records

Hill-Rom Services Pte. Ltd.12596%
Synchrony Medical Ltd43%
Respinnovation11%

Top labelers

CompanyDevicesShare
Hill-Rom Services Pte. Ltd.12596%
Synchrony Medical Ltd43%
Respinnovation11%

Company = labeler of record on GUDID. 3 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

LibAirty Airway Clearance System Vest (L)LibAirty Airway Clearance System Vest (M)LibAirty Airway Clearance System Vest (S)LibAirty Airway Clearance SystemRespInThe Vest®SystemThe MetaNeb®SystemThe VitalCough®SystemThe MetaNeb® SystemThe Vest APX SystemMonarch™ System

Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.

FDA product codes

CodeNameDevices
BYIPERCUSSOR, POWERED-ELECTRIC101
NHJDEVICE, POSITIVE PRESSURE BREATHING, INTERMITTENT24
BYIPercussor, Powered-Electric12
NHJDevice, Positive Pressure Breathing, Intermittent2

GMDN & GCC registration

  • GMDN code 38124 · non‑implantable
  • Single‑use 24% · sterile 0% · Rx‑only 6% · OTC 0%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

No structured size data on the register.

Use these as the dimensions to specify in a tender line.

How many chest-oscillation airway secretion-clearing system products are registered in the US?

130 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Chest-oscillation airway secretion-clearing system", from 3 companies. The largest labeler is Hill-Rom Services Pte. Ltd. with 96% of records.

Which FDA product codes apply?

BYI (PERCUSSOR, POWERED-ELECTRIC), NHJ (DEVICE, POSITIVE PRESSURE BREATHING, INTERMITTENT), BYI (Percussor, Powered-Electric), NHJ (Device, Positive Pressure Breathing, Intermittent)

Is this the same as UAE/GCC registration?

No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.

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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.

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