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Stimpod Nms450x+

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref XT-45030Model STIMPOD NMS450X+

by Xavant Technology (Pty) Ltd

Identity

Trade Name
STIMPOD NMS450X+ EUDAMED
STIMPOD Quantitative NMT Monitor EUDAMED
Xavant Technology FDA UDI
Generic Name
Diagnostic peripheral nerve electrical stimulation system FDA UDI
Device Name
STIMPOD NMS450X+ EUDAMED
STIMPOD NMS450 Quantitative NMT Monitor EUDAMED
The STIMPOD NMS450 is a Quantitative Neuromuscular Blockade monitor. The STIMPOD NMS 450 is also a precision nerve locating tool used for localizing specific neural pathways. FDA UDI
Model / Reference
XT-45030 EUDAMED
STIMPOD NMS450X+ EUDAMED
STIMPOD NMS450 Kit FDA UDI
Description
The STIMPOD NMS450 is a Quantitative Neuromuscular Blockade monitor. The STIMPOD NMS 450 is also a precision nerve locating tool used for localizing specific neural pathways. FDA UDI

Identifiers

Catalog Number
XT-45030 FDA UDI
Primary DI / UDI-DI
06009880396870 EUDAMEDFDA UDI
Basic UDI-DI
B-06009880396870 EUDAMED
510(k) Number
K102084 FDA UDI
FDA Product Code
BXN FDA UDI
EMDN Code
Z12062899 NEUROMUSCULAR STIMULATION EQUIPMENT - OTHER EUDAMED
GMDN Term
Diagnostic peripheral nerve electrical stimulation system FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
868.2775 FDA UDI
Market of Registration
Germany EUDAMED
Austria 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

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

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

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Stimpod Nms450x+ by Xavant Technology (pty) Ltd — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
ZA-MF-000011657
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (3)

  • EUDAMED b84ea0bd-1440-4640-ba68-2db5e70abab7 61 fields · synced Jun 18, 2026
  • FDA UDI 15c1e191-340c-428c-9ee2-2143483999dd 36 fields · synced May 30, 2026
  • EUDAMED 807fcfec-1114-4dfd-9350-229c7586aca3 61 fields · synced Jun 18, 2026