989803164921

GUDID 30884838014542

Philips Medizin Systeme Böblingen GmbH

Pulse oximeter probe, single-use
Primary Device ID30884838014542
NIH Device Record Keyb7c15cf3-cefe-4d24-a860-7bd3fbee0148
Commercial Distribution StatusIn Commercial Distribution
Version Model Number989803164921
Catalog Number989803164921
Company DUNS314101143
Company NamePhilips Medizin Systeme Böblingen GmbH
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

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Device Identifiers

Device Issuing AgencyDevice ID
GS130884838014542 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DQAOximeter

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-11-22

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