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Device Explorer · FDA GUDID · GMDN 46823

PEEP valve, single-use

A non-sterile device used in a respiratory or anaesthesia breathing circuit or system to maintain a selected level of positive end expiratory pressure (PEEP) in a patient's airway during ventilation. The device is typically constructed of plastic and metal mat

US‑registered devices118in commercial distribution
Companies21labelers on GUDID
Single‑use99%of device records
Sterile0%labelled sterile
Prescription95%Rx‑only share
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Share of device records

Galemed Corporation1714%
Besmed Health Business Corp.1614%
Teleflex Incorporated1210%
Respironics Novametrix, Llc119%
Airlife119%
Pulmodyne Inc98%
Ventlab, Llc76%
Sunmed, Llc54%

Top labelers

CompanyDevicesShare
Galemed Corporation1714%
Besmed Health Business Corp.1614%
Teleflex Incorporated1210%
Respironics Novametrix, Llc119%
Airlife119%
Pulmodyne Inc98%
Ventlab, Llc76%
Sunmed, Llc54%
Ambu A/S43%
Westmed, Inc.43%
Mercury Enterprises, Inc.43%
Bound Tree Medical, Llc33%

Company = labeler of record on GUDID. 21 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

The BAG PEEP Valve 5-20 cmH2OThe BAG PEEP Valve 2-10 cmH2ON/ADisposable PEEP 20 ValveDISPOSABLE PEEP VALVE 5-20cmH2O, BLUE, ID:30mmDISPOSABLE PEEP VALVE 2-10cm H2O, ORANGEPEEP VALVE 20cmH2O;STRAIGHT CONNECTORS 30m,22mPEEP VALVE 20cmH2OPEEP VALVE 15cmH2O;STRAIGHT CONNECTORS 30m,22mPEEP VALVE 15cmH2OPEEP VALVE 12.5cmH2O;STRAIGHT CONNECTORS 30m,22mPEEP VALVE 12.5cmH2OPEEP VALVE 10cmH2O;STRAIGHT CONNECTORS 30m,22mPEEP VALVE 10cmH2OPEEP VALVE 7.5cmH2O;STRAIGHT CONNECTORS 30m,22mPEEP VALVE 7.5cmH2O

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

FDA product codes

CodeNameDevices
BYEAttachment, Breathing, Positive End Expiratory Pressure80
BYEAttachment, breathing, positive end expiratory pressure32
BTMVentilator, emergency, manual (resuscitator)12
BTLVentilator, emergency, powered (resuscitator)2
BSJMASK, GAS, ANESTHETIC2
BTMVentilator, Emergency, Manual (Resuscitator)1

GMDN & GCC registration

  • GMDN code 46823 · non‑implantable
  • Single‑use 99% · sterile 0% · Rx‑only 95% · 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

Outer Diameter (Millimeter) · 13Lumen/Inner Diameter (Millimeter) · 10Height (Millimeter) · 4Length (Inch) · 4Length (Millimeter) · 1Weight (Gram) · 1

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

How many peep valve, single-use products are registered in the US?

118 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "PEEP valve, single-use", from 21 companies. The largest labeler is Galemed Corporation with 14% of records.

Which FDA product codes apply?

BYE (Attachment, Breathing, Positive End Expiratory Pressure), BYE (Attachment, breathing, positive end expiratory pressure), BTM (Ventilator, emergency, manual (resuscitator)), BTL (Ventilator, emergency, powered (resuscitator))

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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