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AM MAC-2 Macintosh Blade

FDA UDI

Class I (US FDA UDI)

by Instrumentation Industries, Incorporated

Identity

Trade Name
AM MAC-2 Macintosh Blade FDA UDI
Generic Name
Laryngoscope blade, reusable FDA UDI
Device Name
Curved Macintosh laryngoscope blade Size 2 - 108mm FDA UDI
Model / Reference
AM MAC-2 FDA UDI
Description
Curved Macintosh laryngoscope blade Size 2 - 108mm FDA UDI

Identifiers

Catalog Number
AM MAC-2 FDA UDI
Primary DI / UDI-DI
M996AMMAC20 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

Dimensions & Sizes

Size
Length — 108 Millimeter FDA UDI

Category: Laryngoscope blade, reusable

AM MAC-2 Macintosh Blade by Instrumentation Industries, Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laryngoscope blade, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1dfd5150-b377-412b-bb05-150ebfeef347 36 fields · synced Jun 8, 2026