All-Purpose Arch

FDA UDI

Class II (US FDA UDI)

by NORAS MRI products GmbH

Identity

Trade Name: All-Purpose Arch FDA UDI
Generic Name: MRI system coil, radio-frequency FDA UDI
Model / Reference: 02 FDA UDI

Identifiers

Catalog Number: 113393 FDA UDI
Primary DI / UDI-DI: 04251269205668 FDA UDI
510(k) Number: K071179 FDA UDI
K133506 FDA UDI
FDA Product Code: HBL FDA UDI
MOS FDA UDI
GMDN Term: MRI system coil, radio-frequency FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 882.4460 FDA UDI
892.1000 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Safe FDA UDI

Category: MRI system coil, radio-frequency

All-Purpose Arch by NORAS MRI products GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: NORAS MRI products GmbH

Sources (1)

FDA UDI 23a4d4c1-f32d-4c8a-81a5-5670e3d86a15 35 fields · synced Jun 1, 2026