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3T Loop 7 cm MR coil

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare

Identity

Trade Name
3T 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
08625670 FDA UDI
Description
MRI Coil FDA UDI

Identifiers

Primary DI / UDI-DI
04056869014364 FDA UDI
FDA Product Code
LNI FDA UDI
OUO FDA UDI
LNH FDA UDI
MOS 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
892.1200 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 magnetPET/MRI system

3T 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 PET/MRI system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Siemens Healthcare

Sources (1)

  • FDA UDI 054782e4-6819-4dcc-9372-1db17c8f693d 34 fields · synced Jun 8, 2026