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ReliOn

FDA UDI

Class II (US FDA UDI)

by Walmart Stores

Identity

Trade Name
ReliOn FDA UDI
Generic Name
Sharps container FDA UDI
Device Name
ReliOn Sharps Container FDA UDI
Model / Reference
SC-02QR FDA UDI
Description
ReliOn Sharps Container FDA UDI

Identifiers

Primary DI / UDI-DI
06947462492421 FDA UDI
FDA Product Code
MMK FDA UDI
GMDN Term
Sharps container 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Sharps 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 c3a4f5f3-f72c-4c35-b28b-6555855eb1a4 33 fields · synced Jun 1, 2026