AeroKEE

Primary DI
10850091824002
Brand
AeroKEE
Company
Healkee Medical USA Inc.
Model
HL-AERO-F-1
Catalog number
HL-AERO-F-1
Device description
Single-use, non-sterile, patient-worn endoscopic procedure mask for adult patients during oral or transnasal gastroscopy, bronchoscopy, or nasal endoscopy. Designed to support procedural workflow hygiene through localized management of fluids and droplets at the endoscope insertion site.
Published
2026-09-24
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
false
Sterile
false
Single use
true

Product Codes#

Code, Name table
CodeName
PUIDrape, Surgical, Exempt

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
PUIDrape, Surgical, ExemptGeneral, Plastic Surgery2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
20850091824009PackageGS112In Commercial Distribution
10850091824002PrimaryGS10
00850091824005Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
2085009182400920850091824009
1085009182400210850091824002
00850091824005008500918240058500918240050850091824005

GMDN Terms#

Term, Definition table
TermDefinition
Endoscope face maskA form-shaped mask designed to be placed over the mouth and/or nose of a patient to support hygiene (e.g., containing procedural fluids) during the insertion and removal of an endoscope into the oral and/or nasal cavity. It typically has a transparent window, adjustable straps, a forming nosepiece, and an endoscope entry valve for smooth insertion/removal. This is a single-use device.

Regulatory Flags#

DUNS number
149944835
Device count
8
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
true
Expiration date on label
true
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
10850091824019AeroKEEHL-AERO-C-1HL-AERO-C-12026-09-24

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
10809160538999HalyardMEDICAL ACTION INDUSTRIES INC.PUI2026-09-24
10850091824019AeroKEEHealkee Medical USA Inc.PUI2026-09-24
10197344220083MEDLINEMEDLINE INDUSTRIES, INC.PUI2026-09-18
10197344220090MEDLINEMEDLINE INDUSTRIES, INC.PUI2026-09-18
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