Patient Controlled Intravenous Analgesia Device (PCI) PCIIVRE5

GUDID 09350902000273

GO MEDICAL INDUSTRIES PTY. LTD.

Ambulatory non-insulin infusion pump, mechanical, single-use Ambulatory non-insulin infusion pump, mechanical, single-use Ambulatory non-insulin infusion pump, mechanical, single-use Ambulatory non-insulin infusion pump, mechanical, single-use Ambulatory non-insulin infusion pump, mechanical, single-use
Primary Device ID09350902000273
NIH Device Record Keyaa86b48b-ead4-4a71-bdcd-900206ae60b7
Commercial Distribution StatusIn Commercial Distribution
Brand NamePatient Controlled Intravenous Analgesia Device (PCI)
Version Model NumberPCI
Catalog NumberPCIIVRE5
Company DUNS757634266
Company NameGO MEDICAL INDUSTRIES PTY. LTD.
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 Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS109350902000259 [Primary]
GS109350902000266 [Package]
Contains: 09350902000259
Package: Carton [10 Units]
In Commercial Distribution
GS109350902000273 [Package]
Contains: 09350902000259
Package: Shipping carton [60 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MEBPump, Infusion, Elastomeric

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2022-06-17
Device Publish Date2017-05-18

On-Brand Devices [Patient Controlled Intravenous Analgesia Device (PCI)]

09350902000303PCI Tamper Evident
09350902000273PCI

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