Disposable PEEP 20 valve

FDA UDI

Class II (US FDA UDI)

by Ambu A/S

Identity

Trade Name: Disposable PEEP 20 valve FDA UDI
Generic Name: PEEP valve, single-use FDA UDI
Device Name: Ambu Disposable PEEP valve; 20 pcs/20 mm FDA UDI
Model / Reference: 199002020 FDA UDI
Description: Ambu Disposable PEEP valve; 20 pcs/20 mm FDA UDI

Identifiers

Catalog Number: 199002020 FDA UDI
Primary DI / UDI-DI: 05707480030705 FDA UDI
FDA Product Code: BYE FDA UDI
GMDN Term: PEEP valve, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.5965 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Conditional FDA UDI

Dimensions & Sizes

Size: Weight — 40 Gram FDA UDI
Length — 65 Millimeter FDA UDI
Outer Diameter — 45 Millimeter FDA UDI

Category: PEEP valve, single-use

Disposable PEEP 20 valve by Ambu A/S — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as PEEP valve, single-use.

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AirLife™ — Airlife, Inc. · Class II
Whisperflow CPAP Valve — Respironics Novametrix, LLC · Class II
PEEP VALVE 15cmH2O;STRAIGHT CONNECTORS 30m, 22m — BESMED HEALTH BUSINESS CORP. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Ambu A/S

Sources (1)

FDA UDI 6df66b31-aeff-4078-a91b-a981cbd56abd 37 fields · synced May 31, 2026