Reusable PEEP 10 valve

FDA UDI

Class II (US FDA UDI)

by Ambu A/S

Identity

Trade Name: Reusable PEEP 10 valve FDA UDI
Generic Name: PEEP valve, reusable FDA UDI
Device Name: PEEP 10 valve FDA UDI
Model / Reference: A137001000 FDA UDI
Description: PEEP 10 valve FDA UDI

Identifiers

Catalog Number: A137001000 FDA UDI
Primary DI / UDI-DI: 05707480030668 FDA UDI
FDA Product Code: BYE FDA UDI
GMDN Term: PEEP valve, reusable 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

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 Unsafe FDA UDI

Dimensions & Sizes

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

Category: PEEP valve, reusable

Reusable PEEP 10 valve by Ambu A/S — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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 fbda0cdb-9f81-4226-b2e1-f42fb324f2df 37 fields · synced May 30, 2026