FDA.reportPublic FDA data

reusable resuscitator

Primary DI
04719872104568
Brand
reusable resuscitator
Company
ENTER MEDICAL CORPORATION
Model
ENT-1022
Device description
reusable resuscitator
Published
2023-10-19
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true

Product Codes#

Code, Name table
CodeName
BTMVentilator, Emergency, Manual (Resuscitator)

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
BTMVentilator, Emergency, Manual (Resuscitator)Anesthesiology2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K042556000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K042556000SHINEBALL PVC MANUAL RESUSCIATOR, ENT-1001, ENT-1003, ENT-1005, SHINEBALL SILICONE MANUAL RESUSCIATOR, ENT-1022,Enter Medical Corporation2005-03-11BTM

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
04719872104568PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
04719872104568047198721045684719872104568

GMDN Terms#

Term, Definition table
TermDefinition
Pulmonary resuscitator, manual, reusableA hand-operated device designed to provide or assist ventilation in patients who are apnoeic or exhibit inadequate respiration. It typically employs entrained ambient air and includes a large flexible chamber that is hand-ventilated, a gas reservoir, tubing, and a connector for attachment to a mask or endotracheal (ET) tube; oxygen (O2) from an O2 source may also be connected when necessary. It is used by emergency medical services (EMS) in ambulances, intensive care units (ICU), during internal patient transfer, accident and emergency (A&E), mass casualty incidents (MCI), and is generally placed strategically throughout a hospital. This is a reusable device.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
658833116
Device count
1
Lot or batch
true
Manufacturing date on label
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
04719872100607RESERVOIRPN-06012023-10-19
04719872101208Seal Rite Mask1202023-10-19
04719872102021Catheter MountPN-20252023-10-19
04719872103028Bubble HumidifierPN-302-012023-10-19
04719872104414Nasal CannulaPN-20132023-10-19
04719872109631Disposable ResuscitatorENT-10012023-10-19
04719872109853Anaesthetic Face MaskPN-05062023-10-19
04719872102014Oxygen TubeENT-20232023-09-28
047198721088012M TubeENT-20232023-09-28
04719872109501Breathing CircuitENT-20232023-09-28
04719872109532Breathing CircuitENT-20232023-09-28
04719872109723HEAD STRAPENT-20232023-09-28
04719872102007LARYNGOSCOPEENT-20022023-06-19
04719872103929Silicone maskPN-0503-22A2023-06-19
04719872104124Water TrapENT-20132023-06-19
04719872108764Bite BlockPN-6002023-06-19
04719872108788Berman AirwayPN-20012023-06-19
04719872108795Teeth Screw DriverPN-20022023-06-19
04719872101017mada10282015-10-14
04719872101024mada14342015-10-14

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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10197344097432MEDLINEMEDLINE INDUSTRIES, INC.BTM2025-06-13
10197344097449MEDLINEMEDLINE INDUSTRIES, INC.BTM2025-06-13
10197344100446MEDLINEMEDLINE INDUSTRIES, INC.BTM2025-06-13
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