Manometer Connecting Port

GUDID 30641043553200

MERCURY ENTERPRISES, INC.

Tube/mask breathing circuit connector, single-use, non-sterile Tube/mask breathing circuit connector, single-use, non-sterile Tube/mask breathing circuit connector, single-use, non-sterile Tube/mask breathing circuit connector, single-use, non-sterile Tube/mask breathing circuit connector, single-use, non-sterile Tube/mask breathing circuit connector, single-use, non-sterile Tube/mask breathing circuit connector, single-use, non-sterile Tube/mask breathing circuit connector, single-use, non-sterile Tube/mask breathing circuit connector, single-use, non-sterile Tube/mask breathing circuit connector, single-use, non-sterile Tube/mask breathing circuit connector, single-use, non-sterile Tube/mask breathing circuit connector, single-use, non-sterile Tube/mask breathing circuit connector, single-use, non-sterile Tube/mask breathing circuit connector, single-use, non-sterile Tube/mask breathing circuit connector, single-use, non-sterile Tube/mask breathing circuit connector, single-use, non-sterile Straight/elbow breathing circuit connector, single-use Straight/elbow breathing circuit connector, single-use Straight/elbow breathing circuit connector, single-use Straight/elbow breathing circuit connector, single-use Straight/elbow breathing circuit connector, single-use Straight/elbow breathing circuit connector, single-use Straight/elbow breathing circuit connector, single-use Straight/elbow breathing circuit connector, single-use Straight/elbow breathing circuit connector, single-use Straight/elbow breathing circuit connector, single-use Straight/elbow breathing circuit connector, single-use
Primary Device ID30641043553200
NIH Device Record Keyc854814b-31e3-41c3-8836-68781cee144a
Commercial Distribution StatusIn Commercial Distribution
Brand NameManometer Connecting Port
Version Model Number10-55320
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 Usetrue
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

Phone727-573-0088
Emailhospitalcustomerservice@mercurymed.com
Phone727-573-0088
Emailhospitalcustomerservice@mercurymed.com
Phone727-573-0088
Emailhospitalcustomerservice@mercurymed.com
Phone727-573-0088
Emailhospitalcustomerservice@mercurymed.com
Phone727-573-0088
Emailhospitalcustomerservice@mercurymed.com
Phone727-573-0088
Emailhospitalcustomerservice@mercurymed.com
Phone727-573-0088
Emailhospitalcustomerservice@mercurymed.com
Phone727-573-0088
Emailhospitalcustomerservice@mercurymed.com
Phone727-573-0088
Emailhospitalcustomerservice@mercurymed.com
Phone727-573-0088
Emailhospitalcustomerservice@mercurymed.com
Phone727-573-0088
Emailhospitalcustomerservice@mercurymed.com
Phone727-573-0088
Emailhospitalcustomerservice@mercurymed.com
Phone727-573-0088
Emailhospitalcustomerservice@mercurymed.com
Phone727-573-0088
Emailhospitalcustomerservice@mercurymed.com
Phone727-573-0088
Emailhospitalcustomerservice@mercurymed.com
Phone727-573-0088
Emailhospitalcustomerservice@mercurymed.com
Phone727-573-0088
Emailhospitalcustomerservice@mercurymed.com
Phone727-573-0088
Emailhospitalcustomerservice@mercurymed.com
Phone727-573-0088
Emailhospitalcustomerservice@mercurymed.com
Phone727-573-0088
Emailhospitalcustomerservice@mercurymed.com
Phone727-573-0088
Emailhospitalcustomerservice@mercurymed.com
Phone727-573-0088
Emailhospitalcustomerservice@mercurymed.com
Phone727-573-0088
Emailhospitalcustomerservice@mercurymed.com
Phone727-573-0088
Emailhospitalcustomerservice@mercurymed.com
Phone727-573-0088
Emailhospitalcustomerservice@mercurymed.com
Phone727-573-0088
Emailhospitalcustomerservice@mercurymed.com
Phone727-573-0088
Emailhospitalcustomerservice@mercurymed.com

Device Identifiers

Device Issuing AgencyDevice ID
GS110641043553206 [Primary]
GS130641043553200 [Package]
Contains: 10641043553206
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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