Transducer L12-4

GUDID 00884838061408

Philips Ultrasound, Inc.

Extracorporeal ultrasound imaging transducer, hand-held
Primary Device ID00884838061408
NIH Device Record Key1a141573-da32-464d-8e8a-7293d50f9e85
Commercial Distribution StatusIn Commercial Distribution
Brand NameTransducer L12-4
Version Model Number989605389262
Company DUNS063377717
Company NamePhilips Ultrasound, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100884838061408 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

ITXTransducer, ultrasonic, diagnostic

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2018-11-12
Device Publish Date2016-03-31

On-Brand Devices [Transducer L12-4]

00884838072305989605451171
00884838068759989605434812
00884838067882989605418963
00884838061835989605434811
00884838061644989605427122
00884838061484989605430652
00884838061408989605389262

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.