Scio Four

GUDID 04048675429333

Drägerwerk AG & Co. KGaA

Anaesthetic agent gas monitor, multiple
Primary Device ID04048675429333
NIH Device Record Key45f5c484-995e-4361-b2b5-50e5822730f2
Commercial Distribution StatusIn Commercial Distribution
Brand NameScio Four
Version Model Number6871804
Company DUNS315578914
Company NameDrägerwerk AG & Co. KGaA
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+494518820
Emailinfo@draeger.com
Phone+494518820
Emailinfo@draeger.com
Phone+494518820
Emailinfo@draeger.com
Phone+494518820
Emailinfo@draeger.com
Phone+494518820
Emailinfo@draeger.com
Phone+494518820
Emailinfo@draeger.com
Phone+494518820
Emailinfo@draeger.com
Phone+494518820
Emailinfo@draeger.com
Phone+494518820
Emailinfo@draeger.com
Phone+494518820
Emailinfo@draeger.com
Phone+494518820
Emailinfo@draeger.com
Phone+494518820
Emailinfo@draeger.com
Phone+494518820
Emailinfo@draeger.com
Phone+494518820
Emailinfo@draeger.com
Phone+494518820
Emailinfo@draeger.com
Phone+494518820
Emailinfo@draeger.com
Phone+494518820
Emailinfo@draeger.com

Device Identifiers

Device Issuing AgencyDevice ID
GS104048675429333 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MHXMonitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

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 Date2015-11-04

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04048675564553 - T-piece N for NO-A2024-10-16
04048675564577 - T-piece N for Nebulization2024-10-16

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