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Moxus

FDA UDI

Class II (US FDA UDI)

by Aei Technologies Inc.

Identity

Trade Name
MOXUS FDA UDI
Generic Name
Metabolic measurement trolley FDA UDI
Device Name
Metabolic Measurement System FDA UDI
Model / Reference
MOXUS FDA UDI
Description
Metabolic Measurement System FDA UDI

Identifiers

Catalog Number
150300 FDA UDI
Primary DI / UDI-DI
B9671503000 FDA UDI
510(k) Number
K874663 FDA UDI
FDA Product Code
BZL FDA UDI
GMDN Term
Metabolic measurement trolley FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.1730 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

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Metabolic measurement trolley

Moxus by Aei Technologies Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metabolic measurement trolley.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d4ee8c07-dfb5-4b06-af2e-24b3d4c36872 36 fields · synced May 31, 2026