DEVICE: Integrity Sterilizers (10841736100131)

Device Identifier (DI) Information

Integrity Sterilizers
INTEGRITY 270VP
In Commercial Distribution
INTEGRITY 270VP
SKYTRON LLC
10841736100131
GS1

1
078375583 *Terms of Use
Integrity 270 Vacuum/Gravity Steam Sterilizer, 26.5"W x 37.5"H x 53"D, Power Door Lock, House Steam, Vacuum Pump
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Device Characteristics

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

GMDN

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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?
38671 Steam sterilizer
A mains electricity (AC-powered) device designed for total elimination and/or inactivation of microorganisms from medical devices and related products using pressurized steam (i.e., moist heat) as the sterilizing agent; it is used for products non-sensitive to high temperature, water, or steam. It typically includes a treatment chamber with shelves for device placement, and controls; it may be intended to sterilize wrapped and/or unwrapped devices. The device is available in a variety of shapes and sizes, including stand-alone (bulk) and tabletop units.
Active false
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FDA Product Code

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Product Code Product Code Name
FLE Sterilizer, steam
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FDA Premarket Submission

FDA Premarket Submission Number [?] Supplement Number [?]
K132439 000
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Sterilization

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

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Storage and Handling
Handling Environment Humidity: between 30 and 90 Percent (%) Relative Humidity
Storage Environment Temperature: between 14 and 104 Degrees Fahrenheit
Handling Environment Atmospheric Pressure: between 70 and 106 KiloPascal
Handling Environment Temperature: between 14 and 104 Degrees Fahrenheit
Storage Environment Humidity: between 30 and 90 Percent (%) Relative Humidity
Storage Environment Atmospheric Pressure: between 70 and 106 KiloPascal
Special Storage Condition, Specify: No Condensation
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Clinically Relevant Size

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Size Type Text
No Device Sizes
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Device Record Status

eacd8c1b-ee8a-4147-8862-83047b8ef901
July 06, 2018
3
September 19, 2016
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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
No Package DIs found
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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

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Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

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No
No
None
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Production Identifier(s) in UDI

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No
Yes
No
Yes
No CLOSE

Customer Contact

[?]
+1(800)759-8766
info@skytron.us
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