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PEEP VALVE 2.5cmH2O

FDA UDI

Class II (US FDA UDI)

by Besmed Health Business Corp.

Identity

Trade Name
PEEP VALVE 2.5cmH2O FDA UDI
Generic Name
PEEP valve, single-use FDA UDI
Model / Reference
CT-20100 FDA UDI

Identifiers

Primary DI / UDI-DI
04716770201009 FDA UDI
510(k) Number
K160112 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: PEEP valve, single-use

PEEP VALVE 2.5cmH2O by Besmed Health Business Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as PEEP valve, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d717ea83-05f1-430c-8bc6-f364f9f336d5 33 fields · synced May 30, 2026