Identity
- Trade Name
- ENLIGHT 2100 FDA UDI
- Generic Name
- Thoracic electrical impedance system, tomographic FDA UDI
- Device Name
- ENLIGHT 2100 is a non-invasive, non-radiation medical device that provides information of local impedance variation within a cross-section of a patient’s thorax. This information is presented to the clinician user as an adjunctive tool to other clinical information in order to support the user’s assessment of variations in regional air content within a cross section of a patient’s lungs. It is intended for mechanically ventilated adult patients in a hospital setting, whose thorax perimeter is within the range of 78 -122 cm. FDA UDI
- Model / Reference
- TPL-E2103-0 FDA UDI
- Description
- ENLIGHT 2100 is a non-invasive, non-radiation medical device that provides information of local impedance variation within a cross-section of a patient’s thorax. This information is presented to the clinician user as an adjunctive tool to other clinical information in order to support the user’s assessment of variations in regional air content within a cross section of a patient’s lungs. It is intended for mechanically ventilated adult patients in a hospital setting, whose thorax perimeter is within the range of 78 -122 cm. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 07898966433146 FDA UDI
- 510(k) Number
- DEN170072 FDA UDI
- FDA Product Code
- QEB FDA UDI
- GMDN Term
- Thoracic electrical impedance system, tomographic FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.1505 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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
Category: Thoracic electrical impedance system, tomographic
Enlight 2100 by Timpel S/A — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
DEN170072 also covers:
- ENLIGHT 1810 — Timpel S/A
- ENLIGHT BELT - L – LEFT — Timpel S/A
- ENLIGHT BELT - L – LEFT — Timpel S/A
- ENLIGHT BELT - L – RIGHT — Timpel S/A
- ENLIGHT BELT - L – RIGHT — Timpel S/A
- ENLIGHT BELT - M – LEFT — Timpel S/A
- ENLIGHT BELT - M – LEFT — Timpel S/A
- ENLIGHT BELT - M – RIGHT — Timpel S/A
- ENLIGHT BELT - M – RIGHT — Timpel S/A
- ENLIGHT BELT - S - LEFT — Timpel S/A
- ENLIGHT BELT - S - RIGHT — Timpel S/A
- ENLIGHT BELT - S - RIGHT — Timpel S/A
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Timpel S/A
Sources (1)
- FDA UDI 39e74d5c-8ea6-4371-9d53-674757b3bfb7 34 fields · synced Jun 8, 2026