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Biograph mMR

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare

Identity

Trade Name
Biograph mMR FDA UDI
Generic Name
PET/MRI system FDA UDI
Device Name
MRI-PET Scanner FDA UDI
Model / Reference
10433372 FDA UDI
Description
MRI-PET Scanner FDA UDI

Identifiers

Primary DI / UDI-DI
04056869006741 FDA UDI
510(k) Number
K133226 FDA UDI
K163234 FDA UDI
K200213 FDA UDI
FDA Product Code
OUO FDA UDI
LNI FDA UDI
KPS FDA UDI
LNH FDA UDI
GMDN Term
PET/MRI system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1200 FDA UDI
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: PET/MRI system

Biograph mMR by Siemens Healthcare — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as PET/MRI system.

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 ebc1c1f9-c0e1-4713-b6fe-7eff5140c30c 35 fields · synced May 30, 2026