989803101001

GUDID 20884838006922

Philips Medical Systems

General-purpose patient temperature probe, single-use
Primary Device ID20884838006922
NIH Device Record Key68e20a60-e698-4f06-a2d5-27721784dd5b
Commercial Distribution StatusIn Commercial Distribution
Version Model Number989803101001
Catalog Number989803101001
Company DUNS078628040
Company NamePhilips Medical Systems
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
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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Operating and Storage Conditions

Storage Environment TemperatureBetween -35 Degrees Celsius and 65 Degrees Celsius
Storage Environment TemperatureBetween -35 Degrees Celsius and 65 Degrees Celsius
Storage Environment TemperatureBetween -35 Degrees Celsius and 65 Degrees Celsius
Storage Environment TemperatureBetween -35 Degrees Celsius and 65 Degrees Celsius
Storage Environment TemperatureBetween -35 Degrees Celsius and 65 Degrees Celsius
Storage Environment TemperatureBetween -35 Degrees Celsius and 65 Degrees Celsius
Storage Environment TemperatureBetween -35 Degrees Celsius and 65 Degrees Celsius
Storage Environment TemperatureBetween -35 Degrees Celsius and 65 Degrees Celsius
Storage Environment TemperatureBetween -35 Degrees Celsius and 65 Degrees Celsius
Storage Environment TemperatureBetween -35 Degrees Celsius and 65 Degrees Celsius
Storage Environment TemperatureBetween -35 Degrees Celsius and 65 Degrees Celsius
Storage Environment TemperatureBetween -35 Degrees Celsius and 65 Degrees Celsius
Storage Environment TemperatureBetween -35 Degrees Celsius and 65 Degrees Celsius
Storage Environment TemperatureBetween -35 Degrees Celsius and 65 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS100884838006928 [Unit of Use]
GS120884838006922 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

EZLCATHETER, RETENTION TYPE, BALLOON

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-07-30
Device Publish Date2018-06-29

Devices Manufactured by Philips Medical Systems

10884838000671 - Paper2021-11-18
00884838107199 - PageWriter2021-10-15
20884838013517 - NA2021-10-01
20884838013524 - NA2021-10-01
20884838091782 - Microstream Advance Adult Oral-Nasal CO2 Filter Line2021-08-02
20884838091829 - Microstream Advance Adult-Intermediate Bite Block CO2 Filter Line2021-08-02
20884838091836 - Microstream Advance Adult-Pediatric Intubated CO2 Filter Line2021-08-02
20884838091850 - Microstream Advance Adult-Pediatric Intubated CO2 Filter Line2021-08-02

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