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Stimulating Probes

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref RLBTP150-2.5

by Rhythmlink International, LLC

Identity

Trade Name
Stimulating Probes EUDAMED
Rhythmlink® FDA UDI
Generic Name
Diagnostic peripheral nerve electrical stimulation system FDA UDI
Device Name
Electrical Neuromuscular Stimulating Probes EUDAMED
10 probes, 150mm long, 1.85-2.5mm diameter, 2.3mm ball tip pedicle screw stimulating probe with touch proof connector FDA UDI
Model / Reference
RLBTP150-2.5 EUDAMEDFDA UDI
Description
10 probes, 150mm long, 1.85-2.5mm diameter, 2.3mm ball tip pedicle screw stimulating probe with touch proof connector FDA UDI

Identifiers

Primary DI / UDI-DI
00816312020779 EUDAMEDFDA UDI
Basic UDI-DI
081631202TF002TY EUDAMED
FDA Product Code
ETN FDA UDI
EMDN Code
Z12101106 NEUROLOGICAL STIMULATORS EUDAMED
GMDN Term
Diagnostic peripheral nerve electrical stimulation system FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
874.1820 FDA UDI
Market of Registration
Belgium 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

Yes

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

Category: Point aesthesiometer

Stimulating Probes by Rhythmlink International, LLC — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Point aesthesiometer.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
US-MF-000012131
Authorised Representative
mdi Europa GmbH DE-AR-000006218

Sources (2)

  • EUDAMED 0e8f23f3-9156-4819-8348-b53574b0e97e 61 fields · synced Jun 9, 2026
  • FDA UDI 60b22a8b-187d-4726-a9c9-66247aa0e2d9 34 fields · synced May 30, 2026