← Back to catalogue

Stimpod

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref XT-45003B

by Xavant Technology (pty) Ltd

Identity

Trade Name
NMT Monitoring Cable EMG (3.0m) EUDAMED
STIMPOD FDA UDI
Generic Name
Diagnostic peripheral nerve electrical stimulation system FDA UDI
Device Name
NMT Monitoring Cable EMG EUDAMED
Neuromuscular blocking agent monitoring cable (3.0m) using electromyography. Accessory to be used with the STIMPOD NMS450 Nerve Stimulator. FDA UDI
Model / Reference
XT-45003B EUDAMED
NMT Monitoring Cable EMG (3.0m) FDA UDI
Description
Neuromuscular blocking agent monitoring cable (3.0m) using electromyography. Accessory to be used with the STIMPOD NMS450 Nerve Stimulator. FDA UDI

Identifiers

Catalog Number
XT-45003B FDA UDI
Primary DI / UDI-DI
06009880396177 EUDAMEDFDA UDI
Basic UDI-DI
06009880396XT45003BE EUDAMED
510(k) Number
K213049 FDA UDI
FDA Product Code
BXN FDA UDI
EMDN Code
Z12062880 NEUROMUSCULAR STIMULATION EQUIPMENT - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Diagnostic peripheral nerve electrical stimulation system FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
868.2775 FDA UDI
Market of Registration
Italy EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Diagnostic peripheral nerve electrical stimulation system

Stimpod by Xavant Technology (pty) Ltd — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Diagnostic peripheral nerve electrical stimulation system.

Cleared under the same submission

K213049 also covers:

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Xavant Technology (pty) Ltd

Sources (2)

  • FDA UDI 0ea5f021-36cc-4eee-bed2-a3503bcbd0ba 36 fields · synced Jul 31, 2026
  • EUDAMED e33d130e-70cd-48dc-91a4-ad25d4ac6913 61 fields · synced Jul 31, 2026