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Siemens 3.0T Endo Interface (eCoil®)

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 8624855

by DxTx Medical, Inc.

Identity

Trade Name
Siemens 3.0T Endo Interface (eCoil®) EUDAMED
DxTx Medical 3T eCoil Imaging Device (FRU for Siemens) FDA UDI
Generic Name
MRI system coil, radio-frequency FDA UDI
Device Name
Siemens 3.0T Endo Interface (eCoil®) EUDAMED
Ecoil ID - STID TIM 30 FRU - 8624855 FDA UDI
Model / Reference
8624855 EUDAMED
STID TIM 30 FRU FDA UDI
Description
Ecoil ID - STID TIM 30 FRU - 8624855 FDA UDI

Identifiers

Primary DI / UDI-DI
00850011472187 EUDAMEDFDA UDI
Basic UDI-DI
085001147208624855VM EUDAMED
Direct Marketing DI
00850011472187 EUDAMED
510(k) Number
K051349 FDA UDI
FDA Product Code
MOS FDA UDI
EMDN Code
Z1105018099 MAGNETIC RESONANCE (MR) SYSTEMS - HARDWARE ACCESSORIES - OTHER EUDAMED
GMDN Term
MRI system coil, radio-frequency FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
892.1000 FDA UDI
Market of Registration
Netherlands 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 Conditional FDA UDI

Siemens 3.0T Endo Interface (eCoil®) by Dxtx Medical Inc — Class I — 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

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Manufacturer

Manufacturer
DxTx Medical, Inc.
EUDAMED SRN
US-MF-000026795
Authorised Representative
MedR-AR Services B.V. NL-AR-000000120

Sources (2)

  • EUDAMED 296e440d-0eab-46b9-bc72-43351e608df1 61 fields · synced Jul 15, 2026
  • FDA UDI 07134a07-4db1-4b4f-b658-c59068f78805 34 fields · synced May 30, 2026