HEINE GAMMA® XXL LF M-000.09.323

GUDID 04053755136575

Heine Optotechnik GmbH & Co. KG

Aneroid manual sphygmomanometer Aneroid manual sphygmomanometer Aneroid manual sphygmomanometer Aneroid manual sphygmomanometer Aneroid manual sphygmomanometer Aneroid manual sphygmomanometer Aneroid manual sphygmomanometer Aneroid manual sphygmomanometer Aneroid manual sphygmomanometer Aneroid manual sphygmomanometer Aneroid manual sphygmomanometer Aneroid manual sphygmomanometer Aneroid manual sphygmomanometer Aneroid manual sphygmomanometer Aneroid manual sphygmomanometer
Primary Device ID04053755136575
NIH Device Record Key3df9e675-8004-40f3-a0e3-57d2cbc3ac28
Commercial Distribution StatusIn Commercial Distribution
Brand NameHEINE GAMMA® XXL LF
Version Model Number000
Catalog NumberM-000.09.323
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+1 (603) 742-7103
Emailservice@heine-na.com
Phone+1 (603) 742-7103
Emailservice@heine-na.com
Phone+1 (603) 742-7103
Emailservice@heine-na.com
Phone+1 (603) 742-7103
Emailservice@heine-na.com
Phone+1 (603) 742-7103
Emailservice@heine-na.com
Phone+1 (603) 742-7103
Emailservice@heine-na.com
Phone+1 (603) 742-7103
Emailservice@heine-na.com
Phone+1 (603) 742-7103
Emailservice@heine-na.com
Phone+1 (603) 742-7103
Emailservice@heine-na.com
Phone+1 (603) 742-7103
Emailservice@heine-na.com
Phone+1 (603) 742-7103
Emailservice@heine-na.com
Phone+1 (603) 742-7103
Emailservice@heine-na.com
Phone+1 (603) 742-7103
Emailservice@heine-na.com
Phone+1 (603) 742-7103
Emailservice@heine-na.com
Phone+1 (603) 742-7103
Emailservice@heine-na.com

Device Identifiers

Device Issuing AgencyDevice ID
GS104053755136575 [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 Date2016-09-24

On-Brand Devices [HEINE GAMMA® XXL LF]

04053755190690166
04053755136605000
04053755136575000

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