ACCUTRAY

GUDID 20809160283681

MEDICAL ACTION INDUSTRIES INC.

Epidural anaesthesia set, medicated

• Primary Device ID: 20809160283681
• NIH Device Record Key: 2d8e91c9-a325-436d-a2df-6e77621c77f4
• Commercial Distribution Discontinuation: 2020-07-20
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: ACCUTRAY
• Version Model Number: 5300063B
• 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
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	10809160283684 [Primary]
GS1	20809160283681 [Package]; Contains: 10809160283684; Package: [24 Units]; Discontinued: 2020-07-20; Not in Commercial Distribution

FDA Product Code

• OFT: Spinal epidural anesthesia kit

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-07-21
• Device Publish Date: 2020-05-12

On-Brand Devices [ACCUTRAY]

• 20809160113490: 5200114
• 20809160107390: 5200210A
• 20809160279172: 5200115
• 20809160282219: 5200116
• 20809160283674: 5200225B
• 20809160283667: 5200223B
• 20809160283650: 5200222A
• 20809160283643: 5200221B
• 20809160283636: 5200113B
• 20809160283605: 5200110B
• 20809160283681: 5300063B
• 20809160287931: 5200063B
• 20809160001735: 5200225
• 20809160222925: 5200233
• 20809160222918: 5200259
• 20809160001728: 5200223
• 20809160289836: 5200220B
• 20809160001711: 5200222
• 20809160001704: 5200221
• 20809160001674: 5200113
• 20809160001667: 5200110
• 20809160290887: 5200118
• 20809160283599: 5200210B
• 20809160001773: 5200252
• 20809160001766: 5200251
• 20809160410193: 01-5200065
• 20809160410186: 01-5200112
• 20809160283612: 5200073B