← Back to catalogue

Invia Motion 15 Days Kit 10 x 25 cm

FDA UDI

Class II (US FDA UDI)

by Medela LLC

Identity

Trade Name
Invia Motion 15 Days Kit 10 x 25 cm FDA UDI
Generic Name
Negative-pressure wound therapy system, electric, reusable FDA UDI
Device Name
Invia Motion and Invia Integrated Dressing L Convenience Kit FDA UDI
Model / Reference
101045893 FDA UDI
Description
Invia Motion and Invia Integrated Dressing L Convenience Kit FDA UDI

Identifiers

Primary DI / UDI-DI
30020451458930 FDA UDI
510(k) Number
K172145 FDA UDI
K223388 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

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

Invia Motion 15 Days Kit 10 x 25 cm 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Medela LLC

Sources (1)

  • FDA UDI 17562b5e-5767-4ecf-92c0-5a132e976805 34 fields · synced May 31, 2026