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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 FDA UDI
Device Name
3 mL Syringe with Hypodermic Safety Needle FDA UDI
Model / Reference
8881833558 FDA UDI
Description
3 mL Syringe with Hypodermic Safety Needle FDA UDI

Identifiers

Catalog Number
8881833558 FDA UDI
Primary DI / UDI-DI
10884521005846 FDA UDI
FDA Product Code
FMI FDA UDI
GMDN Term
Metered-delivery hypodermic syringe FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5570 FDA UDI
Commercial Distribution
Not 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
Total Volume — 3 Milliliter FDA UDI
Length — 0.625 Inch FDA UDI

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI b10b9980-34fc-46cf-8654-baddf920cd1b 38 fields · synced Jun 8, 2026