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Megadyne

FDA UDI

Class II (US FDA UDI)

by Megadyne Medical Products, Inc.

Identity

Trade Name
Megadyne FDA UDI
Generic Name
Electromechanical device/system transport trolley FDA UDI
Device Name
Mega Power Cart, unassembled, no top shelf FDA UDI
Model / Reference
1300U FDA UDI
Description
Mega Power Cart, unassembled, no top shelf FDA UDI

Identifiers

Catalog Number
1300U FDA UDI
Primary DI / UDI-DI
10614559105290 FDA UDI
510(k) Number
K050579 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Electromechanical device/system transport trolley FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electromechanical device/system transport trolley

Megadyne by Megadyne Medical Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electromechanical device/system transport trolley.

Cleared under the same submission

K050579 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Megadyne Medical Products, Inc.

Sources (1)

  • FDA UDI cf5cb46a-420e-435d-833a-07372e631f1f 37 fields · synced Jun 9, 2026