Disconnect Wedge

GUDID 30641043553408

MERCURY ENTERPRISES, INC.

Respiratory connector disconnection wedge
Primary Device ID30641043553408
NIH Device Record Key1ab3d895-a4b0-45f4-a443-540548eb2a68
Commercial Distribution StatusIn Commercial Distribution
Brand NameDisconnect Wedge
Version Model Number10-55340
Company DUNS032705659
Company NameMERCURY ENTERPRISES, INC.
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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone7275730088
Emailhospitalcustomerservice@mercurymed.com
Phone7275730088
Emailhospitalcustomerservice@mercurymed.com
Phone7275730088
Emailhospitalcustomerservice@mercurymed.com
Phone7275730088
Emailhospitalcustomerservice@mercurymed.com
Phone7275730088
Emailhospitalcustomerservice@mercurymed.com
Phone7275730088
Emailhospitalcustomerservice@mercurymed.com
Phone7275730088
Emailhospitalcustomerservice@mercurymed.com
Phone7275730088
Emailhospitalcustomerservice@mercurymed.com
Phone7275730088
Emailhospitalcustomerservice@mercurymed.com
Phone7275730088
Emailhospitalcustomerservice@mercurymed.com
Phone7275730088
Emailhospitalcustomerservice@mercurymed.com
Phone7275730088
Emailhospitalcustomerservice@mercurymed.com
Phone7275730088
Emailhospitalcustomerservice@mercurymed.com
Phone7275730088
Emailhospitalcustomerservice@mercurymed.com
Phone7275730088
Emailhospitalcustomerservice@mercurymed.com
Phone7275730088
Emailhospitalcustomerservice@mercurymed.com

Device Identifiers

Device Issuing AgencyDevice ID
GS110641043553404 [Primary]
GS130641043553408 [Package]
Contains: 10641043553404
Package: [50 Units]
In Commercial Distribution

FDA Product Code

BYXTubing, Pressure And Accessories

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-06-02
Device Publish Date2021-05-25

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