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Invia Liberty

FDA UDI

Class II (US FDA UDI)

by Medela LLC

Identity

Trade Name
Invia Liberty FDA UDI
Generic Name
Negative-pressure wound therapy system, electric, reusable FDA UDI
Device Name
Negative Pressure Wound Therapy Powered Suction Pump 087.0000 FDA UDI
Model / Reference
Liberty FDA UDI
Description
Negative Pressure Wound Therapy Powered Suction Pump 087.0000 FDA UDI

Identifiers

Catalog Number
200.2222 FDA UDI
Primary DI / UDI-DI
07612367015578 FDA UDI
510(k) Number
K142626 FDA UDI
K172145 FDA UDI
FDA Product Code
OMP FDA UDI
GMDN Term
Negative-pressure wound therapy system, electric, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4780 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

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Negative-pressure wound therapy system, electric, reusable

Invia Liberty by Medela LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Negative-pressure wound therapy system, electric, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medela LLC

Sources (1)

  • FDA UDI 433f2e2a-80dc-4fa3-a9ec-d8d8d6e77b7b 36 fields · synced May 30, 2026