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Selenia FFDM

FDA UDI

Class II (US FDA UDI)

by Hologic, Inc.

Identity

Trade Name
Selenia FFDM FDA UDI
Generic Name
Stationary mammographic x-ray system, digital FDA UDI
Model / Reference
ASY-01427 FDA UDI

Identifiers

Catalog Number
ASY-01427 FDA UDI
Primary DI / UDI-DI
15420045505964 FDA UDI
PMA Number
P010025 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
Not 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Selenia FFDM by Hologic, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hologic, Inc.

Sources (1)

  • FDA UDI f017aabb-2fab-4fef-adc6-ec63ca2d8f78 35 fields · synced Jun 1, 2026