TACY MEDICAL INC

GUDID 20809160412548

MEDICAL ACTION INDUSTRIES INC.

Arterial/central venous catheterization support/maintenance kit, non-medicated Arterial/central venous catheterization support/maintenance kit, non-medicated Arterial/central venous catheterization support/maintenance kit, non-medicated Arterial/central venous catheterization support/maintenance kit, non-medicated Arterial/central venous catheterization support/maintenance kit, non-medicated Arterial/central venous catheterization support/maintenance kit, non-medicated Arterial/central venous catheterization support/maintenance kit, non-medicated Arterial/central venous catheterization support/maintenance kit, non-medicated Arterial/central venous catheterization support/maintenance kit, non-medicated Arterial/central venous catheterization support/maintenance kit, non-medicated Arterial/central venous catheterization support/maintenance kit, non-medicated Arterial/central venous catheterization support/maintenance kit, non-medicated Arterial/central venous catheterization support/maintenance kit, non-medicated

• Primary Device ID: 20809160412548
• NIH Device Record Key: 8cdc46b9-2545-4756-a106-799462b12e82
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TACY MEDICAL INC
• Version Model Number: 8517
• Company DUNS: 092364462
• Company Name: MEDICAL ACTION INDUSTRIES INC.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: true
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *STORE AT ROOM TEMPERATURE
• Special Storage Condition, Specify: Between 0 and 0
• Special Storage Condition, Specify: Between 0 and 0 *STORE AT ROOM TEMPERATURE
• Special Storage Condition, Specify: Between 0 and 0
• Special Storage Condition, Specify: Between 0 and 0 *STORE AT ROOM TEMPERATURE
• Special Storage Condition, Specify: Between 0 and 0
• Special Storage Condition, Specify: Between 0 and 0 *STORE AT ROOM TEMPERATURE
• Special Storage Condition, Specify: Between 0 and 0
• Special Storage Condition, Specify: Between 0 and 0 *STORE AT ROOM TEMPERATURE
• Special Storage Condition, Specify: Between 0 and 0
• Special Storage Condition, Specify: Between 0 and 0 *STORE AT ROOM TEMPERATURE
• Special Storage Condition, Specify: Between 0 and 0
• Special Storage Condition, Specify: Between 0 and 0 *STORE AT ROOM TEMPERATURE
• Special Storage Condition, Specify: Between 0 and 0
• Special Storage Condition, Specify: Between 0 and 0 *STORE AT ROOM TEMPERATURE
• Special Storage Condition, Specify: Between 0 and 0
• Special Storage Condition, Specify: Between 0 and 0 *STORE AT ROOM TEMPERATURE
• Special Storage Condition, Specify: Between 0 and 0
• Special Storage Condition, Specify: Between 0 and 0 *STORE AT ROOM TEMPERATURE
• Special Storage Condition, Specify: Between 0 and 0
• Special Storage Condition, Specify: Between 0 and 0 *STORE AT ROOM TEMPERATURE
• Special Storage Condition, Specify: Between 0 and 0
• Special Storage Condition, Specify: Between 0 and 0 *STORE AT ROOM TEMPERATURE
• Special Storage Condition, Specify: Between 0 and 0
• Special Storage Condition, Specify: Between 0 and 0 *STORE AT ROOM TEMPERATURE
• Special Storage Condition, Specify: Between 0 and 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	10809160412541 [Primary]
GS1	20809160412548 [Package]; Contains: 10809160412541; Package: [20 Units]; In Commercial Distribution

FDA Product Code

• OWL: Peripheral catheter insertion kit

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-12-05
• Device Publish Date: 2023-11-27

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