McGRATH MAC

FDA UDI

Class I (US FDA UDI)

by Covidien LP

Identity

Trade Name: McGRATH MAC FDA UDI
Generic Name: Video intubation laryngoscope handle/monitor FDA UDI
Device Name: Portable Video Laryngoscope FDA UDI
Model / Reference: DL300-000-000 FDA UDI
Description: Portable Video Laryngoscope FDA UDI

Identifiers

Primary DI / UDI-DI: 10884521582576 FDA UDI
FDA Product Code: CCW FDA UDI
GMDN Term: Video intubation laryngoscope handle/monitor FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 868.5540 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Video intubation laryngoscope handle/monitor

McGRATH MAC by Covidien LP — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Covidien LP

Sources (1)

FDA UDI 8619660f-c387-4d4d-9344-465240e325e3 35 fields · synced May 31, 2026