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Swing Maxi

FDA UDI

Class II (US FDA UDI)

by Medela LLC

Identity

Trade Name
Swing Maxi FDA UDI
Generic Name
Breast pump, electric FDA UDI
Device Name
Double electric, single user breast pump intended to express & collect breast milk FDA UDI
Model / Reference
101043638 FDA UDI
Description
Double electric, single user breast pump intended to express & collect breast milk FDA UDI

Identifiers

Primary DI / UDI-DI
00020451436388 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Breast pump, electric

Swing Maxi by Medela LLC — 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

Manufacturer
Medela LLC

Sources (1)

  • FDA UDI 0c6cc2e1-d609-44f7-8a5a-086150307c83 33 fields · synced May 30, 2026