Monoject 11812705

GUDID 20884521544793

1 mL Syringe with Hypodermic Safety Needle

Cardinal Health, Inc.

Metered-delivery hypodermic syringe

• Primary Device ID: 20884521544793
• NIH Device Record Key: b3bcae3c-ee9e-48bd-a5fd-2b1e56e9ca05
• Commercial Distribution Discontinuation: 2025-12-31
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Monoject
• Version Model Number: 11812705
• Catalog Number: 11812705
• Company DUNS: 080935429
• Company Name: Cardinal Health, Inc.
• 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: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• 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 *
• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *

Device Identifiers

Device Issuing Agency	Device ID
GS1	10884521544796 [Primary]
GS1	20884521544793 [Package]; Contains: 10884521544796; Package: PACK_OR_INNER_PACK [100 Units]; Discontinued: 2025-12-31; In Commercial Distribution
GS1	30884521544790 [Package]; Contains: 10884521544796; Package: CASE [1200 Units]; Discontinued: 2025-12-31; In Commercial Distribution

FDA Product Code

• FMF: Syringe, piston

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2024-11-19
• Device Publish Date: 2016-09-24

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