Identity

Trade Name
Lansinoh FDA UDI
Generic Name
Breast pump, electric FDA UDI
Device Name
The Powered Breast Pump is intended to express and collect the breast milk of a nursing woman for the purpose of feeding the collected milk to a baby FDA UDI
Model / Reference
Compact Wearable Pump FDA UDI
Description
The Powered Breast Pump is intended to express and collect the breast milk of a nursing woman for the purpose of feeding the collected milk to a baby FDA UDI

Identifiers

Catalog Number
53750 FDA UDI
Primary DI / UDI-DI
00044677537506 FDA UDI
510(k) Number
K230469 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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Breast pump, electric

Lansinoh by Lansinoh Laboratories Saglik Gerecleri Tasarim Sanayi Ticaret Ltd Sti — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Breast pump, electric.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 53e075b7-6a5e-41d4-9965-db66bb85f446 36 fields · synced Jun 6, 2026