Magellan 8881866810

GUDID 30884521005659

6 mL Syringe with Hypodermic Safety Needle

Cardinal Health, Inc.

Metered-delivery hypodermic syringe/needle

• Primary Device ID: 30884521005659
• NIH Device Record Key: 667c80ef-887a-4049-b219-0f52d39af6bf
• Commercial Distribution Discontinuation: 2021-07-01
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Magellan
• Version Model Number: 8881866810
• Catalog Number: 8881866810
• 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: true
• Serial Number: false
• 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

Device Dimensions

• Length: 1 Inch
• Total Volume: 6 Milliliter
• Device Size Text, specify: 0
• Length: 1 Inch
• Total Volume: 6 Milliliter
• Device Size Text, specify: 0
• Length: 1 Inch
• Total Volume: 6 Milliliter
• Device Size Text, specify: 0
• Length: 1 Inch
• Total Volume: 6 Milliliter
• Device Size Text, specify: 0
• Length: 1 Inch
• Total Volume: 6 Milliliter
• Device Size Text, specify: 0
• Length: 1 Inch
• Total Volume: 6 Milliliter
• Device Size Text, specify: 0
• Length: 1 Inch
• Total Volume: 6 Milliliter
• Device Size Text, specify: 0
• Length: 1 Inch
• Total Volume: 6 Milliliter
• Device Size Text, specify: 0
• Length: 1 Inch
• Total Volume: 6 Milliliter
• Device Size Text, specify: 0
• Length: 1 Inch
• Total Volume: 6 Milliliter
• Device Size Text, specify: 0
• Length: 1 Inch
• Total Volume: 6 Milliliter
• Device Size Text, specify: 0
• Length: 1 Inch
• Total Volume: 6 Milliliter
• Device Size Text, specify: 0
• Length: 1 Inch
• Total Volume: 6 Milliliter
• Device Size Text, specify: 0
• Length: 1 Inch
• Total Volume: 6 Milliliter
• Device Size Text, specify: 0

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT

Device Identifiers

Device Issuing Agency	Device ID
GS1	10884521005655 [Primary]
GS1	20884521005652 [Package]; Contains: 10884521005655; Package: PACK_OR_INNER_PACK [50 Units]; Not in Commercial Distribution
GS1	30884521005659 [Package]; Contains: 10884521005655; Package: CASE [200 Units]; Not in Commercial Distribution

FDA Product Code

• FMI: Needle, hypodermic, single lumen

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 8
• Public Version Date: 2025-06-10
• Device Publish Date: 2016-10-13

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