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Ventlab

FDA UDI

Class II (US FDA UDI)

by Ventlab Corp.

Identity

Trade Name
Ventlab FDA UDI
Generic Name
Pulmonary resuscitator, manual, single-use FDA UDI
Device Name
AirFlow Adult Resuscitator with Integrated Manometer, B/V Filter, Bag Reservoir, Mask, PEEP Valve, and Gas Sampling Line FDA UDI
Model / Reference
AF5140MBP-E FDA UDI
Description
AirFlow Adult Resuscitator with Integrated Manometer, B/V Filter, Bag Reservoir, Mask, PEEP Valve, and Gas Sampling Line FDA UDI

Identifiers

Catalog Number
AF5140MBP-E FDA UDI
Primary DI / UDI-DI
10889483555729 FDA UDI
FDA Product Code
BTM FDA UDI
GMDN Term
Pulmonary resuscitator, manual, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5915 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

Dimensions & Sizes

Size
Total Volume — 1500 Milliliter FDA UDI

Category: Pulmonary resuscitator, manual, single-use

Ventlab by Ventlab Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pulmonary resuscitator, manual, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ventlab Corp.

Sources (1)

  • FDA UDI cfa2d6ef-4598-4a4a-8cef-e23925911dd1 36 fields · synced Jun 7, 2026