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Bemis

FDA UDI

Class II (US FDA UDI)

by Bemis de México, S.A. de C.V.

Identity

Trade Name
BEMIS FDA UDI
Generic Name
Sharps container FDA UDI
Device Name
5 QUART RED SHARPS CONTAINER FDA UDI
Model / Reference
175 030D FDA UDI
Description
5 QUART RED SHARPS CONTAINER FDA UDI

Identifiers

Catalog Number
175 030D FDA UDI
Primary DI / UDI-DI
10073088161854 FDA UDI
510(k) Number
K953797 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

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
Total Volume — 5 Quart FDA UDI

Category: Sharps container

Bemis by Bemis de México, S.A. de C.V. — 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

Sources (1)

  • FDA UDI 51a01be3-2a43-47fc-a701-c25515d40b88 36 fields · synced May 30, 2026