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Maxcon Sharps container

FDA UDI

Class II (US FDA UDI)

by Ningbo Maxcon Medical Technology Co., Ltd.

Identity

Trade Name
Maxcon Sharps container FDA UDI
Generic Name
Sharps container FDA UDI
Device Name
Disposal sharp container 5 QT FDA UDI
Model / Reference
MA1211 FDA UDI
Description
Disposal sharp container 5 QT FDA UDI

Identifiers

Primary DI / UDI-DI
06970623200054 FDA UDI
510(k) Number
K180984 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
Not 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Maxcon Sharps container by Ningbo Maxcon Medical Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K180984 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ningbo Maxcon Medical Technology Co., Ltd.

Sources (1)

  • FDA UDI 6bd509b5-4234-4ff1-bcab-fcf01aab8582 35 fields · synced May 30, 2026