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103583 LuMon™ Contact Gel Kit

FDA UDI

Class II (US FDA UDI)

by Sentec, Inc.

Identity

Trade Name
103583 LuMon™ Contact Gel Kit FDA UDI
Generic Name
Thoracic electrical impedance system, tomographic FDA UDI
Model / Reference
103583 FDA UDI

Identifiers

Primary DI / UDI-DI
07640121881053 FDA UDI
510(k) Number
K243765 FDA UDI
FDA Product Code
QEB FDA UDI
BZQ FDA UDI
GMDN Term
Thoracic electrical impedance system, tomographic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.1505 FDA UDI
868.2375 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Thoracic electrical impedance system, tomographic

103583 LuMon™ Contact Gel Kit by Sentec, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Thoracic electrical impedance system, tomographic.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sentec, Inc.

Sources (1)

  • FDA UDI f143879e-a2ec-44ae-833f-448561b97798 33 fields · synced May 31, 2026