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1.5T Loop 7 cm MR coil

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare

Identity

Trade Name
1.5T Loop 7 cm MR coil FDA UDI
Generic Name
Full-body MRI system, superconducting magnet FDA UDI
Device Name
MRI Coil FDA UDI
Model / Reference
10185555 FDA UDI
Description
MRI Coil FDA UDI

Identifiers

Primary DI / UDI-DI
04056869014814 FDA UDI
510(k) Number
K121434 FDA UDI
K123938 FDA UDI
K151579 FDA UDI
K153343 FDA UDI
FDA Product Code
MOS FDA UDI
LNI FDA UDI
LNH FDA UDI
GMDN Term
Full-body MRI system, superconducting magnet FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1000 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Full-body MRI system, superconducting magnet

1.5T Loop 7 cm MR coil by Siemens Healthcare — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Full-body MRI system, superconducting magnet.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Siemens Healthcare

Sources (1)

  • FDA UDI 3417916a-2b45-4a1b-8f59-8221b3dc21b1 35 fields · synced Jun 6, 2026