TONOPORT BP CUFF ADULT SMALL

GUDID 00742832731522

PAR Medizintechnik GmbH & Co. KG

Blood pressure cuff, reusable
Primary Device ID00742832731522
NIH Device Record Key5686f907-c646-469e-92bf-2ca5a7c8cb89
Commercial Distribution StatusIn Commercial Distribution
Brand NameTONOPORT BP CUFF ADULT SMALL
Version Model Number2001589-211
Company DUNS324233626
Company NamePAR Medizintechnik 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 Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latextrue
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100742832731522 [Primary]

FDA Product Code

DXQBlood Pressure Cuff

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-07-22
Device Publish Date2016-06-13

Devices Manufactured by PAR Medizintechnik GmbH & Co. KG

04260671372547 - blood pressure cuff, Size XS, for digital devices2020-12-29
04260671372554 - blood pressure cuff, Size S, for digital devices2020-12-29
14260671372568 - blood pressure cuff, Size M, for digital devices2020-12-29
14260671372575 - blood pressure cuff, Size L, for digital devices2020-12-29
14260671372582 - blood pressure cuff, Size XL, for digital devices2020-12-29
14260671372599 - blood pressure cuff, Size XXL, for digital devices2020-12-29
04260671372004 - TONOPORT BP Cuff for Adults, Small2020-03-16
04260671372011 - TONOPORT BP Cuff for Adults, Standard2020-03-16

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.