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PEEP 1unit for UDI for 845040

FDA UDI

Class II (US FDA UDI)

by Laerdal Medical Corp.

Identity

Trade Name
PEEP 1unit for UDI for 845040 FDA UDI
Generic Name
PEEP valve, single-use FDA UDI
Device Name
The Laerdal Disposable PEEP Valve Assembly is a single patient use accessory for use with all models of Laerdal brand resuscitators to enable clinicians to apply and adjust the level of PEEP therapy being administered to a patient. The PEEP Valve connector is the standard 30 mm ID size FDA UDI
Model / Reference
20-09502 FDA UDI
Description
The Laerdal Disposable PEEP Valve Assembly is a single patient use accessory for use with all models of Laerdal brand resuscitators to enable clinicians to apply and adjust the level of PEEP therapy being administered to a patient. The PEEP Valve connector is the standard 30 mm ID size FDA UDI

Identifiers

Catalog Number
20-09502 FDA UDI
Primary DI / UDI-DI
07045432068696 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
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

PEEP 1unit for UDI for 845040 by Laerdal Medical Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Laerdal Medical Corp.

Sources (1)

  • FDA UDI e543ad51-17cb-45d7-81ac-a4bdfcc4687f 37 fields · synced Jun 8, 2026