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Lvb

FDA UDI

Class II (US FDA UDI)

by Huizhou LVB Maternal & Infant Supplies Co., Ltd.

Identity

Trade Name
LVB FDA UDI
Generic Name
Breast pump, electric FDA UDI
Device Name
Wearable Breast Pump FDA UDI
Model / Reference
K2 FDA UDI
Description
Wearable Breast Pump FDA UDI

Identifiers

Primary DI / UDI-DI
06935883919023 FDA UDI
510(k) Number
K241004 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Breast pump, electric

Lvb by Huizhou LVB Maternal & Infant Supplies Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Breast pump, electric.

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 c34f4eae-3552-4388-8dcc-bed2673c4955 34 fields · synced May 30, 2026