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Whole body - removable table

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare

Identity

Trade Name
Whole body - removable table FDA UDI
Generic Name
Full-body MRI system, superconducting magnet FDA UDI
Device Name
MRI Patient Table FDA UDI
Model / Reference
08108248 FDA UDI
Description
MRI Patient Table FDA UDI

Identifiers

Primary DI / UDI-DI
04056869022710 FDA UDI
510(k) Number
K121434 FDA UDI
K123938 FDA UDI
FDA Product Code
LNH FDA UDI
LNI 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
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

Whole body - removable table 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 3b77e1f7-7644-43f7-af15-5309515aa791 35 fields · synced Jun 8, 2026