Macintosh (A) LED Blade

FDA UDI

Class I (US FDA UDI)

by Maco International

Identity

Trade Name: Macintosh (A) LED Blade FDA UDI
Generic Name: Laryngoscope blade, reusable FDA UDI
Model / Reference: LA4462-1 FDA UDI

Identifiers

Catalog Number: LA4462-1 FDA UDI
Primary DI / UDI-DI: G272LA446210 FDA UDI
FDA Product Code: CCW FDA UDI
GMDN Term: Laryngoscope blade, reusable 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

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

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Laryngoscope blade, reusable

Macintosh (A) LED Blade by Maco International — 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: Maco International

Sources (1)

FDA UDI 1d38a283-8d6f-4400-b932-d0fbe9adf1d2 33 fields · synced Jun 6, 2026