Identity
- Trade Name
- ENLIGHT ADDERE - XXS FDA UDI
- Generic Name
- Thoracic electrical impedance electrode array conductive skin adhesive tape FDA UDI
- Device Name
- Addere is a disposable accessory that envelopes the electrode belt and works as the interface between the electrode belt and the patient’s body. Biocompatible, non- invasive and latex-free accessory in different sizes for adult and pediatric patients, designed for exclusive use with ENLIGHT Electrode Belts. Non-sterile and not to be sterilized. FDA UDI
- Model / Reference
- AD-03005-1 FDA UDI
- Description
- Addere is a disposable accessory that envelopes the electrode belt and works as the interface between the electrode belt and the patient’s body. Biocompatible, non- invasive and latex-free accessory in different sizes for adult and pediatric patients, designed for exclusive use with ENLIGHT Electrode Belts. Non-sterile and not to be sterilized. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 07898959841163 FDA UDI
- 510(k) Number
- K211135 FDA UDI
- FDA Product Code
- QEB FDA UDI
- GMDN Term
- Thoracic electrical impedance electrode array conductive skin adhesive tape 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
Yes
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Thoracic electrical impedance electrode array conductive skin adhesive tape
Enlight Addere - Xxs by Timpel S/A — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Thoracic electrical impedance electrode array conductive skin adhesive tape.
- ENLIGHT ELECTRODE ADDERE- SIZE 4S — Timpel S/A · Class II
- ENLIGHT ELECTRODE ADDERE- SIZE L — Timpel S/A · Class II
- ENLIGHT ADDERE - 4S — Timpel S/A · Class II
- ENLIGHT ELECTRODE ADDERE - SIZE M — Timpel S/A · Class II
- ENLIGHT ELECTRODE ADDERE- SIZE S — Timpel S/A · Class II
- ENLIGHT ADDERE - 5S — Timpel S/A · Class II
- ENLIGHT ELECTRODE ADDERE- SIZE XS — Timpel S/A · Class II
- ENLIGHT ADDERE - P2 — Timpel S/A · Class II
Cleared under the same submission
K211135 also covers:
- ENLIGHT 2100 — Timpel S/A
- ENLIGHT ADDERE - 4S — Timpel S/A
- ENLIGHT ADDERE - 5S — Timpel S/A
- ENLIGHT ADDERE - P0 — Timpel S/A
- ENLIGHT ADDERE - P1 — Timpel S/A
- ENLIGHT ADDERE - P2 — Timpel S/A
- ENLIGHT ADDERE - XL — Timpel S/A
- ENLIGHT BELT - 4S - LEFT — Timpel S/A
- ENLIGHT BELT - 4S - RIGHT — Timpel S/A
- ENLIGHT BELT - 5S - LEFT — Timpel S/A
- ENLIGHT BELT - 5S - RIGHT — Timpel S/A
- ENLIGHT BELT - L - LEFT — 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Timpel S/A
Sources (1)
- FDA UDI c8999b88-90e1-4938-badd-e7f84cdb7b8f 34 fields · synced May 30, 2026