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Moore Medical

FDA UDI

Class II (US FDA UDI)

by Moore Medical Corp.

Identity

Trade Name
Moore Medical FDA UDI
Generic Name
Sharps container FDA UDI
Device Name
Sharps 10Qt Btl Red MMC FDA UDI
Model / Reference
93263 FDA UDI
Description
Sharps 10Qt Btl Red MMC FDA UDI

Identifiers

Primary DI / UDI-DI
10607415001898 FDA UDI
510(k) Number
K942054 FDA UDI
FDA Product Code
FMI 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

Moore Medical by Moore Medical Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sharps container.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Moore Medical Corp.

Sources (1)

  • FDA UDI 1297a29e-6fe4-4713-96d8-60b71a5adcf1 34 fields · synced Jun 1, 2026