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Moore

FDA UDI

Class II (US FDA UDI)

by Moore Medical Corp.

Identity

Trade Name
Moore FDA UDI
Generic Name
Cardiopulmonary resuscitation mask, reusable FDA UDI
Device Name
CPR Mask w/Filter & O2 Moore FDA UDI
Model / Reference
73509 FDA UDI
Description
CPR Mask w/Filter & O2 Moore FDA UDI

Identifiers

Primary DI / UDI-DI
10607415001416 FDA UDI
FDA Product Code
CBP FDA UDI
GMDN Term
Cardiopulmonary resuscitation mask, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5870 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

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cardiopulmonary resuscitation mask, reusable

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

Similar devices

Also classified as Cardiopulmonary resuscitation mask, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Moore Medical Corp.

Sources (1)

  • FDA UDI e8430497-73bc-47f7-82db-11e44467ba5e 33 fields · synced May 30, 2026