Sharp Trap

GUDID B594ST1000

HARBOR SAFETY PRODUCTS INC

Sharps container
Primary Device IDB594ST1000
NIH Device Record Keya821a290-269f-49eb-9857-92c1cc323d2e
Commercial Distribution StatusIn Commercial Distribution
Brand NameSharp Trap
Version Model NumberST100
Company DUNS129731373
Company NameHARBOR SAFETY PRODUCTS 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 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
HIBCCB594ST1000 [Primary]

FDA Product Code

MMKContainer, Sharps

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-03-25
Device Publish Date2017-11-02

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