Mam

FDA UDI

Class II (US FDA UDI)

by Mam USA Corporation

Identity

Trade Name: MAM FDA UDI
Generic Name: Breast pump, electric FDA UDI
Device Name: Electric Double Breast Pump (model KP053_01) FDA UDI
Model / Reference: 6100 FDA UDI
Description: Electric Double Breast Pump (model KP053_01) FDA UDI

Identifiers

Catalog Number: 6100-006-2-1 FDA UDI
Primary DI / UDI-DI: 00845296061003 FDA UDI
FDA Product Code: HGX FDA UDI
GMDN Term: Breast pump, electric FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 884.5160 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Breast pump, electric

Mam by Mam USA Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Mam USA Corporation

Sources (1)

FDA UDI f7234265-978e-4d81-b7d4-f7fe9e403c1e 34 fields · synced Jun 8, 2026