Petroleum Gauze Dressing, Non-Woven

GUDID 00840117324213

Med-High Absorbency For wound stages 2, 3, 4 Sterile

DYNAREX CORPORATION

Petrolatum non-woven gauze pad Petrolatum non-woven gauze pad Petrolatum non-woven gauze pad Petrolatum non-woven gauze pad Petrolatum non-woven gauze pad Petrolatum non-woven gauze pad Petrolatum non-woven gauze pad Petrolatum non-woven gauze pad Petrolatum non-woven gauze pad Petrolatum non-woven gauze pad Petrolatum non-woven gauze pad Petrolatum non-woven gauze pad Petrolatum non-woven gauze pad Petrolatum non-woven gauze pad Petrolatum non-woven gauze pad Petrolatum non-woven gauze pad
Primary Device ID00840117324213
NIH Device Record Key01e78868-2d8b-466b-9f1f-1b081a35cbb2
Commercial Distribution StatusIn Commercial Distribution
Brand NamePetroleum Gauze Dressing, Non-Woven
Version Model Number3041
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 Batchfalse
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
GS100840117324206 [Package]
Package: Box [12 Units]
In Commercial Distribution
GS100840117324213 [Primary]
GS100840117324220 [Package]
Contains: 00840117324206
Package: Case [6 Units]
In Commercial Distribution

FDA Product Code

NADDressing, Wound, Occlusive

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-09-14
Device Publish Date2022-09-06

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