1st Chocie

GUDID 00819856022025

AMMEX CORPORATION

Nitrile examination/treatment glove, non-powdered, non-antimicrobial

• Primary Device ID: 00819856022025
• NIH Device Record Key: db3ea5a8-b75e-4b94-9cd5-caada32a36fe
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 1st Chocie
• Version Model Number: 1MEBNLBX2
• Company DUNS: 187070768
• Company Name: AMMEX CORPORATION
• 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: 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00819856022025 [Primary]

FDA Product Code

• LZA: Polymer Patient Examination Glove

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: 2023-07-06
• Device Publish Date: 2023-06-28

On-Brand Devices [1st Chocie]

• 10819856022220: 1ENSCS2
• 00819856022025: 1MEBNLBX2
• 00819856020519: pallet of 50