Codonics Safe Label System®(SLS) 550i Point of Care Station - 144C

GUDID 00814905020823

Integrated computer based barcode scan & print system automatically to verify drugs & print labels of prepared drugs & other items-144C

CODONICS INC.

Anaesthesia unit, mobile

• Primary Device ID: 00814905020823
• NIH Device Record Key: 688d8ba4-dd27-4b5a-85dd-e9e8996ebeab
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Codonics Safe Label System®(SLS) 550i Point of Care Station - 144C
• Version Model Number: 550i PCS
• Company DUNS: 101533727
• Company Name: CODONICS INC.
• Device Count: 1
• DM Exempt: false
• 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: false
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 4402431334
• Email: support@codonics.com
• Phone: 4402431334
• Email: support@codonics.com
• Phone: 4402431334
• Email: support@codonics.com
• Phone: 4402431334
• Email: support@codonics.com
• Phone: 4402431334
• Email: support@codonics.com
• Phone: 4402431334
• Email: support@codonics.com
• Phone: 4402431334
• Email: support@codonics.com
• Phone: 4402431334
• Email: support@codonics.com
• Phone: 4402431334
• Email: support@codonics.com
• Phone: 4402431334
• Email: support@codonics.com
• Phone: 4402431334
• Email: support@codonics.com
• Phone: 4402431334
• Email: support@codonics.com
• Phone: 4402431334
• Email: support@codonics.com
• Phone: 4402431334
• Email: support@codonics.com
• Phone: 4402431334
• Email: support@codonics.com
• Phone: 4402431334
• Email: support@codonics.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00814905020823 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K101439

FDA Product Code

• BSZ: Gas-Machine, Anesthesia

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-11-05
• Device Publish Date: 2018-10-05

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