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ReliOn

FDA UDI

Class II (US FDA UDI)

by Walmart Stores

Identity

Trade Name
ReliOn FDA UDI
Generic Name
Autoinjector needle FDA UDI
Device Name
Bonus Pack: 50 Insulin Pen Needles plus 1 Sharps Container FDA UDI
Model / Reference
194346270651 FDA UDI
Description
Bonus Pack: 50 Insulin Pen Needles plus 1 Sharps Container FDA UDI

Identifiers

Primary DI / UDI-DI
00194346270651 FDA UDI
FDA Product Code
FMI FDA UDI
MMK FDA UDI
GMDN Term
Autoinjector 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

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

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

Category: Autoinjector needleSharps container

ReliOn by Walmart Stores — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sharps container.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Walmart Stores

Sources (1)

  • FDA UDI 5574123b-28a8-4cd0-b7ca-9ab12ef9cd2e 33 fields · synced Jun 8, 2026