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Vacuum gun-adapter for PP system for Invivo Multi Hub Assembly

FDA UDI

Class II (US FDA UDI)

by NORAS MRI products GmbH

Identity

Trade Name
Vacuum gun-adapter for PP system for Invivo Multi Hub Assembly FDA UDI
Generic Name
MRI system coil, radio-frequency FDA UDI
Device Name
The intended use of MR-BI320-PA 1.5T/3T is, in conjunction with a Magnetic Resonance Scanner, the MR examination of the female breast. FDA UDI
Model / Reference
01 FDA UDI
Description
The intended use of MR-BI320-PA 1.5T/3T is, in conjunction with a Magnetic Resonance Scanner, the MR examination of the female breast. FDA UDI

Identifiers

Catalog Number
MR10062-MHA FDA UDI
Primary DI / UDI-DI
04251269207266 FDA UDI
510(k) Number
K081118 FDA UDI
K082373 FDA UDI
FDA Product Code
MOS FDA UDI
GMDN Term
MRI system coil, radio-frequency 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

Yes

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: MRI system coil, radio-frequency

Vacuum gun-adapter for PP system for Invivo Multi Hub Assembly by NORAS MRI products GmbH — Class II — FDA UDI — listed in FDA GUDID

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 137285bc-e938-4ea1-b8d8-81ec47e6e183 36 fields · synced May 30, 2026