MULTI-FLEX 6.0 X 26 CM

GUDID 00821925007239

Gyrus Acmi, Inc.

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Primary Device ID00821925007239
NIH Device Record Key7389a85b-7f24-4f11-86d1-b26421542d56
Commercial Distribution StatusIn Commercial Distribution
Brand NameMULTI-FLEX 6.0 X 26 CM
Version Model Number5476260
Company DUNS007198742
Company NameGyrus Acmi, Inc.
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100821925007239 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FADSTENT, URETERAL

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-10-03

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00810008180983 - nCare2023-10-02 nCare, D, DRCT SDI, ELA, DICOM, RCRDG

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