1st Choice

GUDID 00819856020328

Box

AMMEX CORPORATION

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

• Primary Device ID: 00819856020328
• NIH Device Record Key: 5edec351-62f5-42af-8109-545920da4fb7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 1st Choice
• Version Model Number: 1EINXL
• 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	00819856020328 [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: 2022-07-29
• Device Publish Date: 2022-07-21

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• 10819856022251: 1ENXLCS2
• 10819856022244: 1ENLCS2
• 10819856022237: 1ENMCS2
• 00819856021424: 1ENXLBX2
• 00819856021417: 1ENLBX2
• 00819856021400: 1ENMBX2
• 00819856021394: 1ENSBX2
• 00819856020984: pallet of 70
• 00819856020977: pallet of 70
• 00819856020960: pallet of 70
• 00819856020953: pallet of 70
• 10819856022336: 1MEBNXLCS2
• 10819856022329: 1MEBNLCS2
• 10819856022312: 1MEBNMCS2
• 10819856022305: 1MEBNSCS2
• 00819856022032: 1MEBNXLBX2
• 00819856022018: 1MEBNMBX2
• 00819856022001: 1MEBNSBX2