momcozy

FDA UDI

Class II (US FDA UDI)

by Shenzhen Lutejiacheng Technology Co., Ltd.

Identity

Trade Name: momcozy FDA UDI
Generic Name: Breast pump, electric FDA UDI
Device Name: The Wearable Breast Pump is intended to express milk from lactating women in order to collect breast milk from their breasts. The device is intended for a single user. FDA UDI
Model / Reference: S9 Pro-purple FDA UDI
Description: The Wearable Breast Pump is intended to express milk from lactating women in order to collect breast milk from their breasts. The device is intended for a single user. FDA UDI

Identifiers

Primary DI / UDI-DI: 06975740360582 FDA UDI
510(k) Number: K230776 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

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Breast pump, electric

momcozy by Shenzhen Lutejiacheng Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K230776 also covers:

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: Shenzhen Lutejiacheng Technology Co., Ltd.

Sources (1)

FDA UDI 8fcf59f8-b531-476c-af34-16d3934b138a 35 fields · synced Jun 1, 2026