DEVICE: PLUS (00810050860697)

Device Identifier (DI) Information

PLUS
P5401-01-004
In Commercial Distribution

LIFEPORT, LLC
00810050860697
GS1

1
556196210 *Terms of Use
PLUS, 48 IN BAY WITH 6 IN CANTILEVER STRUC
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Device Characteristics

Labeling does not contain MRI Safety Information
No
No
No
No
No
No
No
No

GMDN

[?]

GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.

GMDN Term Code GMDN Term Name GMDN Term Definition GMDN Term Status [?] Implantable?
60489 Ambulance stretcher docking device
A device designed to be installed within an ambulance to facilitate the manual docking and locking of an ambulance stretcher to an ambulance, and secure the stretcher during transportation. It consists of a docking point(s) that may include a manual lifting/guiding mechanism.
Active false
58008 Laboratory pump, vacuum
A mains electricity (AC-powered) pump designed for use in a laboratory to produce vacuum. It is typically used to support many laboratory activities/processes such as sample aspiration, separation, and drying. It has an electric motor typically connected to a rotating or membrane-type pump head that removes (sucks in) air to produce strong suction (vacuum). It is typically used to aspirate liquids from samples in various types of containers (e.g., microplates, test tubes), draw liquids through a filter, and create vacuum in containers.
Active false
31253 Medical device air compressor
A mains electricity (AC-powered) device designed to create compressed air and supply it directly to gas-powered or compressed air dependent devices (e.g., ventilators or other respiratory devices, laboratory equipment). It may also provide medical air depending upon the filtering systems employed.
Active false
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FDA Product Code

[?]
Product Code Product Code Name
FOX Stand, Infusion
BTI Compressor, Air, Portable
GCX Apparatus, Suction, Operating-Room, Wall Vacuum Powered
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FDA Premarket Submission

FDA Premarket Submission Number [?] Supplement Number [?]
Premarket Submission Number Not Available/Not Released
Yes CLOSE

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 Record Status

eb7dfd06-4c43-4179-9456-efe9bfc50c7c
May 19, 2021
1
May 11, 2021
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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
No Package DIs found
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Secondary DI

[?]
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

[?]
No
Yes
No
Yes
No CLOSE

Customer Contact

[?]
360-225-1212
CustomerService@lifeport.com
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