FDA.reportPublic FDA data

McGrath MAC Blade Size X3

Primary DI
00884521214630
Brand
McGrath MAC Blade Size X3
Company
AIRCRAFT MEDICAL LTD.
Model
X3-003-000
Device description
McGrath MAC Blade Size X3
Published
2022-06-13
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
CCWLARYNGOSCOPE, RIGID

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
CCWLaryngoscope, RigidAnesthesiology1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00884521214081PackageGS110Not in Commercial Distribution
00884521214630PackageGS110Not in Commercial Distribution
10884521184565PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00884521214081008845212140818845212140810884521214081
00884521214630008845212146308845212146300884521214630
1088452118456510884521184565

GMDN Terms#

Term, Definition table
TermDefinition
Laryngoscope blade, single-useThe segment of a laryngoscope (i.e., rigid intubation type) intended to be inserted into the oral cavity to manipulate the tongue, preventing it from obstructing the oropharynx and enabling a clear view of the trachea for the insertion of an endotracheal (ET) tube prior to the delivery of inhalation anaesthesia and/or ventilation. It is connected to the laryngoscope handle and illumination of the airway is provided by a small built-in light bulb or a fibreoptic light. This device may be curved or straight and of various designs and lengths; it may be hinged/interchanged with the handle. Some types are magnetic resonance imaging (MRI) compatible. This is a single-use device.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+1(508)261-8000covidien.udi@covidien.com

Regulatory Flags#

DUNS number
222254083
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
true
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
20884521824345McGRATH MAC350-072-0002023-06-19
30884521824311McGRATH MAC350-005-0002022-09-25
30884521816347McGRATH MAC350-072-0002022-06-13
20884521824369McGRATH MAC350-086-0002022-02-05
30884521824380McGRATH MAC350-084-0002022-02-05
30884521824397McGRATH MAC350-082-0002022-02-06
20884521824376McGRATH MAC350-088-0002022-01-27
25060272980324McGRATH MAC350-013-0002022-01-17
30884521824328McGRATH MAC350-013-0002021-10-30
30884521816316McGRATH MAC350-005-0002021-10-21
20884521816333McGRATH MAC350-017-0002021-10-18
20884521824154McGRATH340-000-0002021-10-07
25060272980065McGRATH340-000-0002021-10-07
25060272980126McGRATH340-200-0002021-10-07
20884521823393McGRATH MAC301-000-0002021-09-30
20884521824352McGRATHX3-003-0002021-09-01
30884521816323McGRATH MAC350-013-0002021-08-30
20884521824338McGRATH MAC350-017-0002021-08-26
25060272980317McGRATH MAC350-005-0002021-08-02
25060272980027McGRATH MAC300-000-0002021-07-05

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