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Bemis

FDA UDI

Class II (US FDA UDI)

by Bemis Manufacturing Co.

Identity

Trade Name
BEMIS FDA UDI
Generic Name
Sharps container FDA UDI
Device Name
11 GALLON YELLOW SHARPS CONTAINER WITH DUAL PURPOSE LID FDA UDI
Model / Reference
111 040 FDA UDI
Description
11 GALLON YELLOW SHARPS CONTAINER WITH DUAL PURPOSE LID FDA UDI

Identifiers

Catalog Number
111 040 FDA UDI
Primary DI / UDI-DI
10073088148886 FDA UDI
510(k) Number
K950340 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 — 8 Gallon FDA UDI

Category: Sharps container

Bemis by Bemis Manufacturing Co. — 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 8ff71218-b4cc-454b-accf-51a5cfd4d745 36 fields · synced May 31, 2026