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Invia Motion Carrying Case

FDA UDI

Class II (US FDA UDI)

by Medela LLC

Identity

Trade Name
Invia Motion Carrying Case FDA UDI
Generic Name
Personal device holder, reusable FDA UDI
Model / Reference
087.4003 FDA UDI

Identifiers

Primary DI / UDI-DI
07612367060509 FDA UDI
510(k) Number
K161128 FDA UDI
K172145 FDA UDI
FDA Product Code
OMP FDA UDI
GMDN Term
Personal device holder, 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Personal device holder, reusable

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

Similar devices

Also classified as Personal device holder, 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 434f00fc-901c-4606-b8c3-5ac313d305f9 34 fields · synced Jun 6, 2026