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Lansinoh Manual Breast Pump

FDA UDI

Class I (US FDA UDI)

by Lansinoh Laboratories Saglik Gerecleri Tasarim Sanayi Ticaret Ltd Sti

Identity

Trade Name
Lansinoh Manual Breast Pump FDA UDI
Generic Name
Breast pump, manual FDA UDI
Device Name
The Non-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
MBP 1.0 FDA UDI
Description
The Non-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
50520 FDA UDI
Primary DI / UDI-DI
20044677505202 FDA UDI
FDA Product Code
HGY FDA UDI
GMDN Term
Breast pump, manual FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.5150 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Breast pump, manual

Lansinoh Manual Breast Pump by Lansinoh Laboratories Saglik Gerecleri Tasarim Sanayi Ticaret Ltd Sti — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Breast pump, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5102df6a-b683-4313-921f-83bddb1e186b 35 fields · synced May 29, 2026