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WaterPAP Pro

FDA UDI

Class II (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
WaterPAP Pro FDA UDI
Generic Name
PEEP valve, single-use FDA UDI
Device Name
WaterPAP Pro (10 devices in one box. 10 boxes in one case) FDA UDI
Model / Reference
WP-7800 FDA UDI
Description
WaterPAP Pro (10 devices in one box. 10 boxes in one case) FDA UDI

Identifiers

Primary DI / UDI-DI
00709078013201 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

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

Yes

FDA UDI

Category: PEEP valve, single-use

WaterPAP Pro by Westmed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as PEEP valve, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Westmed, Inc.

Sources (1)

  • FDA UDI 6af254c9-e6e1-4da3-aac4-e9e04b61146d 33 fields · synced May 30, 2026