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MicroDose SI

FDA UDI

Class II (US FDA UDI)

by Philips Digital Mammography Sweden AB

Identity

Trade Name
MicroDose SI FDA UDI
Generic Name
Stationary mammographic x-ray system, digital FDA UDI
Device Name
Philips MicroDose Mammography SI L50 is intended to produce radiographic images of the human breast for the purpose of diagnostic and screening mammography. The system is intended to be used in the same clinical applications as traditional film-based mammography systems. FDA UDI
Model / Reference
L50 FDA UDI
Description
Philips MicroDose Mammography SI L50 is intended to produce radiographic images of the human breast for the purpose of diagnostic and screening mammography. The system is intended to be used in the same clinical applications as traditional film-based mammography systems. FDA UDI

Identifiers

Catalog Number
714048 FDA UDI
Primary DI / UDI-DI
00884838070943 FDA UDI
FDA Product Code
MUE FDA UDI
GMDN Term
Stationary mammographic x-ray system, digital FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1715 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: Stationary mammographic x-ray system, digital

MicroDose SI by Philips Digital Mammography Sweden AB — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stationary mammographic x-ray system, digital.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4614fee8-ebbd-4191-92cf-e74dfb702ec0 34 fields · synced May 30, 2026