← Back to catalogue

Urethral electrode

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref UE006

by Spes Medica S.p.A.

Identity

Trade Name
Urethral electrode EUDAMED
Urethral Catheter Electrode FDA UDI
Generic Name
Urodynamic measurement system FDA UDI
Device Name
Stimulation and recording electrodes for pelvic floor EUDAMED
Model / Reference
UE006 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
18054655026013 EUDAMEDFDA UDI
Basic UDI-DI
8054655000005XY EUDAMED
FDA Product Code
FAP FDA UDI
EMDN Code
N010101 ELECTROMYOGRAPHIC ELECTRODES EUDAMED
GMDN Term
Urodynamic measurement system FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
876.1620 FDA UDI
Market of Registration
Italy 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

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

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

Urethral electrode by Spes Medica S.p.A. — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Spes Medica S.p.A.
EUDAMED SRN
IT-MF-000008858

Sources (2)

  • EUDAMED 94ce5364-3d97-47b4-9525-334cc979300b 61 fields · synced Jun 18, 2026
  • FDA UDI eefee07b-13bd-4306-8bc6-808bef51ca0b 32 fields · synced May 30, 2026