DNAP Electrode
by Ad-Tech Medical Instrument Corporation
510(k) K152547Ref DNAP-01-05X
DNAP Electrode is a device classified as Class III in the EU and Class II in the US made by Ad-Tech Medical Instrument Corporation, registered in EUDAMED on 5 Nov 2026 (Basic UDI-DI B-00841823106629), cleared under FDA 510(k) K152547 on 4 Mar 2016 and listed in FDA GUDID since 3 Oct 2016 (UDI-DI 00841823106629), active as of 7 Nov 2026.
Active
CE MDD 510(k)
Valid until
No date given
FDA recalls
None found
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD EUDAMED | NumberB-00841823106629 00841823106629 | Date5 Nov 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00841823106629 | Date3 Oct 2016 | StatusListed |
| United States | FDA 510(k)SESE 510(k) | NumberK152547 | Date4 Mar 2016 | StatusActive |
Official records
- EUDAMED public site B-00841823106629
- AccessGUDID record 00841823106629
- FDA 510(k) database K152547
Across registries
- EUDAMED Basic UDI-DI B-00841823106629 registered 5 Nov 2026 Active
- FDA 510(k) K152547 decided 4 Mar 2016 Active
- FDA GUDID UDI-DI 00841823106629 listed 3 Oct 2016 Listed
Timeline
- Cleared FDA 510(k) K152547
- Listed FDA GUDID 00841823106629
- Registered EUDAMED B-00841823106629
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Cortical electrode
- Device name
- Cranial Nerve Electrode
- Model / Ref / Catalog
- DNAP-01-05X
- Primary DI / UDI-DI
- 00841823106629
- Basic UDI-DI
- B-00841823106629
- 510(k) Number
- FDA product code
- GZL 510(k)GYC GUDID
- EMDN code
- N010101 Electromyographic electrodes
- GMDN term
- Cortical electrode
- Device class
- Class III EUDAMEDClass II 510(k)GUDID
- Regulation
- 21 CFR Part 882.1330 510(k)882.1310 GUDID
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Ireland
- Advisory committee
- Neurology
- FDA decision
- SESE Substantially Equivalent
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | 510(k) | GUDID |
|---|---|---|---|
| FDA product code | — | GZL | GYC |
| Device class | Class III | Class II | Class II |
| Regulation number | — | 882.1330 | 882.1310 |
Devices cleared under K152547
Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.
| UDI-DI | Size and differences | |||
|---|---|---|---|---|
| DNAP Electrode DNAP-01-05X | DNAP-01-05X / DNAP-01-05X | 00841823106629 | — | On the market |
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