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Broselow™

FDA UDI

Class II (US FDA UDI)

by Airlife, Inc.

Identity

Trade Name
BROSELOW™ FDA UDI
Generic Name
Cardiopulmonary resuscitation kit, single-use FDA UDI
Device Name
BROSELOW™ IV DELIVERY MODULES FDA UDI
Model / Reference
7700RIV FDA UDI
Description
BROSELOW™ IV DELIVERY MODULES FDA UDI

Identifiers

Catalog Number
7700RIV FDA UDI
Primary DI / UDI-DI
10889483589007 FDA UDI
FDA Product Code
OKI FDA UDI
GMDN Term
Cardiopulmonary resuscitation kit, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4040 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cardiopulmonary resuscitation kit, single-use

Broselow™ by Airlife, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiopulmonary resuscitation kit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Airlife, Inc.

Sources (1)

  • FDA UDI c6bbac76-cea8-4d8e-81d3-8e233a78821b 35 fields · synced Jun 8, 2026