DEVICE: BE 105-2X22 Adapter (M996BE1052X220)
Device Identifier (DI) Information
BE 105-2X22 Adapter
BE 105-2X22
In Commercial Distribution
BE 105-2X22
INSTRUMENTATION INDUSTRIES, INCORPORATED
BE 105-2X22
In Commercial Distribution
BE 105-2X22
INSTRUMENTATION INDUSTRIES, INCORPORATED
General Adapter - 22mm ID x 22mm ID adapter for use in breathing/ventilator circuit. Molded of polycarbonate. Reusable.
Device Characteristics
Labeling does not contain MRI Safety Information | |
No | |
Yes | |
No | |
No | |
Yes | |
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? |
---|---|---|---|---|
42601 | Straight/elbow breathing circuit connector, reusable |
A device intended to create a direct connection between a breathing circuit breathing tube and an endotracheal (ET) tube, anaesthesia face mask, or other non-sampling breathing circuit component. It is constructed with specific connecting dimensions and may be designed to connect breathing tubes from paediatric to adult sizes. It is typically made of plastic materials and can have a straight or elbow-shaped design (excludes 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 reusable device.
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Active | false |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
CAI | Circuit, Breathing (W Connector, Adaptor, Y Piece) |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
---|---|
Premarket Submission Number Not Available/Not Released |
Sterilization
No
Yes
CLOSE
Yes
Sterilization Method [?] |
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Radiation Sterilization |
Ethylene Oxide |
High-level Disinfectant |
Storage and Handling
[?]Storage and Handling |
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No storage/handling found |
Clinically Relevant Size
[?]Size Type Text |
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No Device Sizes |
Device Record Status
37a83c07-00bf-41eb-890c-8f8eef8ef045
November 28, 2022
6
July 21, 2017
November 28, 2022
6
July 21, 2017
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
---|---|---|---|---|---|
M996BE1052X224 | 25 | M996BE1052X220 | In Commercial Distribution | Ziplock bag | |
M996BE1052X221 | 5 | M996BE1052X220 | In Commercial Distribution | Ziplock bag |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
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No Secondary DIs found |
Unit of Use DI
[?]
Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
412-854-1133
raqa@iiimedical.com
raqa@iiimedical.com