← Back to catalogue

The Electrode Store

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref PRO-EE6XModel OL5100048

by Impulse Medical Technologies, Inc.

Identity

Trade Name
MedCare Visions EUDAMED
The Electrode Store FDA UDI
Generic Name
Subdermal needle electrode FDA UDI
Device Name
Disposable Sterile EEG Subdermal Needle Electrode EUDAMED
Disposable Subdermal EEG Needle Electrodes 12mm x 29ga Steel, 6 Color Set FDA UDI
Model / Reference
PRO-EE6X EUDAMEDFDA UDI
OL5100048 EUDAMED
Description
Disposable Subdermal EEG Needle Electrodes 12mm x 29ga Steel, 6 Color Set FDA UDI

Identifiers

Catalog Number
PRO-EE6X FDA UDI
Primary DI / UDI-DI
00816022023633 EUDAMEDFDA UDI
Basic UDI-DI
B-00816022023633 EUDAMED
510(k) Number
K020910 FDA UDI
FDA Product Code
GXZ FDA UDI
EMDN Code
N01010202 EEG EXTRACRANIC ELECTRODES EUDAMED
GMDN Term
Subdermal needle electrode FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
882.1350 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Subdermal needle electrode

The Electrode Store by Impulse Medical Technologies, Inc. — Class II — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Subdermal needle electrode.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (2)

  • FDA UDI 98fba139-37ca-4230-8ea5-216a524c64a4 35 fields · synced Jul 25, 2026
  • EUDAMED 37eee19d-dde6-4643-ab46-fd2e3ae94f1e 61 fields · synced Jul 25, 2026