DEVICE: Invasive VentPack Mini (04048675421054)

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Device Identifier (DI) Information

Invasive VentPack Mini
MP01671

Drägerwerk AG & Co. KGaA
04048675421054
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
Tube/mask breathing circuit connector, non-sterile, single-use A non-sterile device intended to connect a breathing circuit to an endotracheal (ET) tube, anaesthesia face mask, or other breathing circuit component. It can be used to connect breathing tubes from adult to paediatric sizes because it is designed with connections whose outer and inner dimensions are standardized by ISO to 22 mm and 15 mm. It is typically made of plastic materials and can have a straight or elbow-shaped design (excluding Y-piece connectors). Some designs may allow for partial rotation at the point of connection (a swivel) and may include a suction port or gas sampling port. This is a single-use device.
Heat/moisture exchanger/microbial filter, non-sterile A non-sterile device intended to be placed within a breathing circuit proximal to the patient, to remove and retain microbes whilst capturing the patient's exhaled heat and moisture so that they can be used to heat and humidify the therapeutic gases inspired by the patient. It is typically a plastic housing which contains both a bidirectional microbial filter, intended to reduce the risk of cross-contamination between patients, and a heat/moisture exchanger (HME), intended to maintain the mucous membranes of the respiratory tract. It is typically used during anaesthesia or periods of prolonged respiratory support/therapy. 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

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Package DI Number Quantity per Package Contains DI Package Package Discontinue Date Package Status Package Type
04048675252474 10 04048675421054 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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