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Magellan

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Magellan FDA UDI
Generic Name
Metered-delivery hypodermic syringe/needle FDA UDI
Device Name
12 mL Syringe with Hypodermic Safety Needle FDA UDI
Model / Reference
8881822115 FDA UDI
Description
12 mL Syringe with Hypodermic Safety Needle FDA UDI

Identifiers

Catalog Number
8881822115 FDA UDI
Primary DI / UDI-DI
10884521005549 FDA UDI
FDA Product Code
FMI FDA UDI
GMDN Term
Metered-delivery hypodermic syringe/needle FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5570 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 1.50 Inch FDA UDI
Total Volume — 12 Milliliter FDA UDI

Category: Metered-delivery hypodermic syringe/needle

Magellan by Cardinalhealth — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metered-delivery hypodermic syringe/needle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI c4a40f19-4e46-4dfc-87dd-0aff2d95ddf2 37 fields · synced Jun 8, 2026