DEVICE: APack Flex Adult,CS Mask Mint5 (04048675420996)

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Device Identifier (DI) Information

APack Flex Adult,CS Mask Mint5
MP01681

Drägerwerk AG & Co. KGaA
04048675420996
GS1
1
No description.
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Device Characteristics

MR Unsafe
No
No
Yes
No
No
No
No
No

GMDN

[?]

GMDN Names and Definitions: © Copyright GMDN Agency 2015. Reproduced with Permission from the GMDN Agency.

GMDN Preferred Term Name GMDN Definition
Microbial medical gas filter, non-sterile, single-use A non-sterile screening device intended to remove microbes from medical gases to prevent patient exposure during respiration, anaesthesia and/or endoscopy; it has no additional non-filtering functions. It is a small plastic housing containing a filter which will typically also filter other particulates (e.g., scale). This is a single-use device.
Gas-sampling/monitoring respiratory tubing, single-use, non-sterile A non-sterile length of flexible tube(s) primarily intended to be used as an interface between tube/mask breathing circuit connector and a measuring instrument [e.g., a carbon dioxide (C02) or multi-gas analyser, manometer/pressure monitor]. It may be intended for pressure monitoring and/or gas sampling but does not include any components intended for delivery of medical gas to the patient; a microbial filter may be included. This is a single-use device.
Anaesthesia face mask, single-use A flexible, form-shaped device designed to be placed over a patient's nose and/or mouth to direct anaesthetic gases to the upper airway. It is made of conductive or non-conductive rubber, polyvinyl chloride (PVC), or other sterilizable materials that produce a soft, flexible cover to create an airtight seal against the patient's face. It typically includes a 22 mm connector (adult) or a 15 mm connector (paediatric), and is available in a range of sizes. It may be stabilized with a headstrap. This device is sometimes used in association with a manual resuscitator. This is a single-use device.
Anaesthesia breathing circuit, single-use, non-sterile A non-sterile assembly of devices designed to conduct medical gases from the fresh gas supply outlet of an anaesthesia unit/workstation to the patient, typically connecting the patient, a ventilator/ventilation bag, carbon dioxide (CO2) absorber, and a monitor. It typically includes both an inhalation and exhalation route and consists of breathing tubes, a ventilation and/or reservoir bag(s), a Y-piece, connectors/adaptors, and gas sampling ports. The absorber, a one-way directional valve, and adjustable pressure limiting (APL) valve are also devices typically employed in the circuit but may not be a part of this device. This is a single-use device.
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FDA Product Code

[?]
Product Code Product Code Name
CAI Circuit, Breathing (W Connector, Adaptor, Y Piece)
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Sterilization

No
No
Sterilization Method [?]
No Sterilization Methods Found
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Storage and Handling

[?]
Storage and Handling
No storage/handling found
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Clinically Relevant Size

[?]
Size Type Text
No Device Sizes
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Device Status

In Commercial Distribution
October 24, 2015

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Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]
Package DI Number Quantity per Package Contains DI Package Package Discontinue Date Package Status Package Type
04048675252450 5 04048675420996 In Commercial Distribution
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Secondary DI

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Issuing Agency [?] Secondary DI Number
No Secondary DIs found
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Unit of Use DI

[?]
Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]
No
No
None
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Production Identifier(s) in UDI

[?]
Yes
No
Yes
Yes
No CLOSE

Customer Contact

[?]
+494518820
info@draeger.com
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