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Base Plate

FDA UDI

Class II (US FDA UDI)

by NORAS MRI products GmbH

Identity

Trade Name
Base Plate FDA UDI
Generic Name
MRI system coil, radio-frequency FDA UDI
Model / Reference
01 FDA UDI

Identifiers

Catalog Number
117260 FDA UDI
Primary DI / UDI-DI
04251269200922 FDA UDI
510(k) Number
K133506 FDA UDI
FDA Product Code
MOI FDA UDI
GMDN Term
MRI system coil, radio-frequency FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.6010 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: MRI system coil, radio-frequency

Base Plate by NORAS MRI products GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as MRI system coil, radio-frequency.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 52735d02-37dc-4e5b-9b94-ba419e2594fb 35 fields · synced May 29, 2026