Obstetrical Kit

GUDID 00616784490236

DYNAREX CORPORATION

Obstetrical/gynaecological surgical procedure kit, medicated
Primary Device ID00616784490236
NIH Device Record Key42d2dd1f-71af-4f2b-a637-aa94ee332ad5
Commercial Distribution StatusIn Commercial Distribution
Brand NameObstetrical Kit
Version Model Number4902
Company DUNS008124539
Company NameDYNAREX CORPORATION
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100616784490229 [Primary]
GS100616784490236 [Package]
Contains: 00616784490229
Package: [10 Units]
In Commercial Distribution

FDA Product Code

KNAInstrument, Manual, Specialized Obstetric-Gynecologic

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

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 [Obstetrical Kit]

006167844902364902
006167844901374901

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