Tubing

GUDID 00847946021719

DUAL LUMEN NIBP TUBING ASSEMBLY, 5 FT

Zoll Medical Corporation

Rechargeable professional automated external defibrillator
Primary Device ID00847946021719
NIH Device Record Key067f5d77-6cdd-4121-be02-fc89607471b2
Commercial Distribution StatusIn Commercial Distribution
Brand NameTubing
Version Model Number3007-0002-02
Company DUNS055363428
Company NameZoll Medical Corporation
Device Count1
DM Exempttrue
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 Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Operating and Storage Conditions

Storage Environment TemperatureBetween 0 Degrees Celsius and 0 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 0 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 0 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 0 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS100847946021719 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DXNSYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE

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 Date2016-09-16

On-Brand Devices [Tubing]

00847946021719DUAL LUMEN NIBP TUBING ASSEMBLY, 5 FT
00847946021702DUAL LUMEN NIBP TUBING ASSEMBLY

Trademark Results [Tubing]

Mark Image

Registration | Serial
Company
Trademark
Application Date
TUBING
TUBING
73518151 not registered Dead/Abandoned
S.A. HOLDITCH & ASSOCIATES, INC.
1985-01-18

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