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Munchkin

FDA UDI

Class I (US FDA UDI)

by Munchkin Inc.

Identity

Trade Name
Munchkin FDA UDI
Generic Name
Breast pump, manual FDA UDI
Device Name
Munchkin Silicone Breast Pump FDA UDI
Model / Reference
MKFE0923 Rev 1 FDA UDI
Description
Munchkin Silicone Breast Pump FDA UDI

Identifiers

Catalog Number
38185 FDA UDI
Primary DI / UDI-DI
00735282381850 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

Yes

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Breast pump, manual

Munchkin by Munchkin Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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

Manufacturer
Munchkin Inc.

Sources (1)

  • FDA UDI fc6df7a6-0fe2-4321-b982-24baf7df5a25 35 fields · synced Jun 8, 2026