HEINE GAMMA® G5 M-000.09.230

GUDID 04053755190706

Heine Optotechnik GmbH & Co. KG

Aneroid manual sphygmomanometer
Primary Device ID04053755190706
NIH Device Record Key97cd135f-3644-4704-984a-1fdefd574103
Commercial Distribution StatusIn Commercial Distribution
Brand NameHEINE GAMMA® G5
Version Model Number166
Catalog NumberM-000.09.230
Company DUNS315274563
Company NameHeine Optotechnik GmbH & Co. KG
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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 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+498152380
Emailinfo@heine.com
Phone+498152380
Emailinfo@heine.com
Phone+498152380
Emailinfo@heine.com
Phone+498152380
Emailinfo@heine.com
Phone+498152380
Emailinfo@heine.com
Phone+498152380
Emailinfo@heine.com
Phone+498152380
Emailinfo@heine.com
Phone+498152380
Emailinfo@heine.com
Phone+498152380
Emailinfo@heine.com
Phone+498152380
Emailinfo@heine.com
Phone+498152380
Emailinfo@heine.com
Phone+498152380
Emailinfo@heine.com
Phone+498152380
Emailinfo@heine.com
Phone+498152380
Emailinfo@heine.com
Phone+498152380
Emailinfo@heine.com

Device Identifiers

Device Issuing AgencyDevice ID
GS104053755190706 [Primary]

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 Number2
Public Version Date2018-03-29
Device Publish Date2017-11-03

On-Brand Devices [HEINE GAMMA® G5]

04053755190706166
04053755136339000
04053755136285000

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