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Magellan

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Magellan FDA UDI
Generic Name
Hypodermic needle, single-use FDA UDI
Device Name
Safety Needle FDA UDI
Model / Reference
7777850215 FDA UDI
Description
Safety Needle FDA UDI

Identifiers

Catalog Number
7777850215 FDA UDI
Primary DI / UDI-DI
10884521155527 FDA UDI
FDA Product Code
FMI FDA UDI
GMDN Term
Hypodermic needle, single-use 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

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 1.50 Inch FDA UDI

Category: Hypodermic needle, single-use

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

Similar devices

Also classified as Hypodermic needle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI d1d2db5f-ae30-4739-a901-a1d7c24b53a8 37 fields · synced Jun 8, 2026