Crosstex International SCK

GUDID 10732224109265

Sure Check Strip

STERITEC PRODUCT MFG. CO., INC.

Surgical/medical respirator, single-use Surgical/medical respirator, non-antimicrobial, single-use Surgical/medical respirator, non-antimicrobial, single-use Surgical/medical respirator, non-antimicrobial, single-use Surgical/medical respirator, non-antimicrobial, single-use Surgical/medical respirator, non-antimicrobial, single-use Surgical/medical respirator, non-antimicrobial, single-use Surgical/medical respirator, non-antimicrobial, single-use Surgical/medical respirator, non-antimicrobial, single-use Surgical/medical respirator, non-antimicrobial, single-use Surgical/medical respirator, non-antimicrobial, single-use Surgical/medical respirator, non-antimicrobial, single-use Surgical/medical respirator, non-antimicrobial, single-use Surgical/medical respirator, non-antimicrobial, single-use Surgical/medical respirator, non-antimicrobial, single-use Surgical/medical respirator, non-antimicrobial, single-use Surgical/medical respirator, non-antimicrobial, single-use Surgical/medical respirator, non-antimicrobial, single-use

• Primary Device ID: 10732224109265
• NIH Device Record Key: 9b65100b-edf9-43d7-b042-ea22a02715f1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Crosstex International
• Version Model Number: SCK
• Catalog Number: SCK
• Company DUNS: 622223196
• Company Name: STERITEC PRODUCT MFG. CO., INC.
• Device Count: 100
• DM Exempt: true
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(888)276-7783
• Email: crosstex@crosstex.com
• Phone: +1(888)276-7783
• Email: crosstex@crosstex.com
• Phone: +1(888)276-7783
• Email: crosstex@crosstex.com
• Phone: +1(888)276-7783
• Email: crosstex@crosstex.com
• Phone: +1(888)276-7783
• Email: crosstex@crosstex.com
• Phone: +1(888)276-7783
• Email: crosstex@crosstex.com
• Phone: +1(888)276-7783
• Email: crosstex@crosstex.com
• Phone: +1(888)276-7783
• Email: crosstex@crosstex.com
• Phone: +1(888)276-7783
• Email: crosstex@crosstex.com
• Phone: +1(888)276-7783
• Email: crosstex@crosstex.com
• Phone: +1(888)276-7783
• Email: crosstex@crosstex.com
• Phone: +1(888)276-7783
• Email: crosstex@crosstex.com
• Phone: +1(888)276-7783
• Email: crosstex@crosstex.com
• Phone: +1(888)276-7783
• Email: crosstex@crosstex.com
• Phone: +1(888)276-7783
• Email: crosstex@crosstex.com
• Phone: +1(888)276-7783
• Email: crosstex@crosstex.com
• Phone: +1(888)276-7783
• Email: crosstex@crosstex.com
• Phone: +1(888)276-7783
• Email: crosstex@crosstex.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00732224109268 [Unit of Use]
GS1	10732224109265 [Primary]

FDA Product Code

• JOJ: Indicator, physical/chemical sterilization process

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-05-06
• Device Publish Date: 2016-10-13

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• 10814434021640 - Getinge Assured Green Tape 1": 2022-06-17
• 30814434021231 - Getinge Assured MI Steam Migrating Integrator Strip: 2020-07-27
• 10732224109265 - Crosstex International: 2020-05-06Sure Check Strip
• 10732224109265 - Crosstex International: 2020-05-06 Sure Check Strip
• 20814434020619 - Getinge Pack Self-Seal Sterilization Pouch 9cm x 13cm: 2019-11-08
• 20814434020626 - Getinge Pack Self-Seal Sterilization Pouch 9cm x 23cm: 2019-11-08