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PA 36 MR coil set 1.5T 098

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare

Identity

Trade Name
PA 36 MR coil set 1.5T 098 FDA UDI
Generic Name
PET/MRI system FDA UDI
Device Name
Contains Medical Device Mat. 10496542 (GTIN:04056869014906) FDA UDI
Model / Reference
10185542 FDA UDI
Description
Contains Medical Device Mat. 10496542 (GTIN:04056869014906) FDA UDI

Identifiers

Primary DI / UDI-DI
04056869014715 FDA UDI
510(k) Number
K151579 FDA UDI
K153343 FDA UDI
FDA Product Code
MOS FDA UDI
LNI FDA UDI
LNH FDA UDI
GMDN Term
PET/MRI system 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: PET/MRI system

PA 36 MR coil set 1.5T 098 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 dba7ac5b-284b-463c-a9b8-25f76fc3a1a4 35 fields · synced May 30, 2026