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Pristina Paddle

FDA UDI

Class I (US FDA UDI)

by Ge Medical Systems, Inc.

Identity

Trade Name
Pristina Paddle FDA UDI
Generic Name
Stationary mammographic x-ray system, digital FDA UDI
Device Name
24x29 STANDARD PADDLE - labelled FDA UDI
Model / Reference
24x29 STD FDA UDI
Description
24x29 STANDARD PADDLE - labelled FDA UDI

Identifiers

Primary DI / UDI-DI
00195278527882 FDA UDI
510(k) Number
K162268 FDA UDI
FDA Product Code
FMQ FDA UDI
GMDN Term
Stationary mammographic x-ray system, digital FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6760 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

Yes

FDA UDI

Category: Stationary mammographic x-ray system, digital

Pristina Paddle by Ge Medical Systems, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

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 6a366a37-313b-45d5-a591-bdac16e98109 35 fields · synced May 30, 2026