Health Care Technology

GUDID 20809160392772

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 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: 20809160392772
• NIH Device Record Key: aec9d26b-c082-449d-a8b3-fc3ea2c826be
• Commercial Distribution Discontinuation: 2023-10-25
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Health Care Technology
• Version Model Number: HCT5975OK-1
• 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
• 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	10809160392775 [Primary]
GS1	20809160392772 [Package]; Contains: 10809160392775; Package: [50 Units]; Discontinued: 2023-10-25; Not in Commercial Distribution

FDA Product Code

• PEZ: Central venous catheter dressing change kit

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2023-10-26
• Device Publish Date: 2023-01-27

On-Brand Devices [Health Care Technology]

• 20809160394219: HCT100CHG
• 20809160396244: HCT5525PX-2
• 20809160396411: HCT900CHX-1
• 20809160398606: HCT-2057-2
• 20809160399740: HCT300CHG
• 20809160401856: HCT1919PICC
• 20809160401573: HCT1919PORT
• 20809160404451: HCT5975OK-2
• 20809160404444: HCT4975OK-NH1
• 20809160409609: HCT8428CP
• 20809160392772: HCT5975OK-1
• 20809160392758: HCT4975OK-NH
• 20809160392765: HCT6057CP-3
• 20809160410575: HCT6057CP-4
• 20809160410568: HCT8874VA-3
• 20809160412043: HCT7478PIV-3
• 20809160394103: HCT7478PIV-2
• 20809160414443: HCT1919PICC-1