GUDID 00697077003005

Amico Diagnostic Incorporated

Blood pressure cuff, reusable Blood pressure cuff, reusable Blood pressure cuff, reusable Blood pressure cuff, reusable Blood pressure cuff, reusable Blood pressure cuff, reusable Blood pressure cuff, reusable Blood pressure cuff, reusable Blood pressure cuff, reusable Blood pressure cuff, reusable Blood pressure cuff, reusable Blood pressure cuff, reusable Blood pressure cuff, reusable Blood pressure cuff, reusable Blood pressure cuff, reusable Blood pressure cuff, reusable Blood pressure cuff, reusable
Primary Device ID00697077003005
NIH Device Record Keydaef583b-fd43-42fb-82a5-4c5aa042a7f6
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberCR2-LF10B-2SF
Company DUNS203163290
Company NameAmico Diagnostic Incorporated
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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 Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100697077003005 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DXQBlood Pressure Cuff

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-08-04
Device Publish Date2023-07-27

Devices Manufactured by Amico Diagnostic Incorporated

00697077002237 - NA2023-08-04
00697077002985 - NA2023-08-04
00697077002992 - NA2023-08-04
00697077003005 - NA2023-08-04
00697077003005 - NA2023-08-04
00697077003012 - NA2023-08-04
00697077002978 - NA2023-07-13
00697077002961 - NA2023-04-26
00697077002923 - NA2022-02-10

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