MDM SPAIN MODEL

GUDID 00816711020660

MDM SPAIN MODEL

PARKER-HANNIFIN CORPORATION

Inhalational analgesia unit
Primary Device ID00816711020660
NIH Device Record Keyfb3beb25-aa77-4b96-8497-fe42d1cbb663
Commercial Distribution StatusIn Commercial Distribution
Brand NameMDM SPAIN MODEL
Version Model Number94500150SPAIN
Company DUNS004175550
Company NamePARKER-HANNIFIN CORPORATION
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 Usefalse
Lot Batchfalse
Serial Numbertrue
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
GS100816711020660 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

BSZGas-Machine, Anesthesia

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2017-08-31

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