YOMEI MOXA

GUDID 04979844114074

YAMASHO CO.,LTD.

Moxa
Primary Device ID04979844114074
NIH Device Record Keyae6c0764-9073-4151-ba44-06a6a6a9ab13
Commercial Distribution StatusIn Commercial Distribution
Brand NameYOMEI MOXA
Version Model Number200g
Company DUNS703173450
Company NameYAMASHO CO.,LTD.
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 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
GS104979844114074 [Primary]

FDA Product Code

IMAPack, Heat, Moist

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-12-08
Device Publish Date2022-11-30

On-Brand Devices [YOMEI MOXA]

04979844114074200g
04979844114067100g

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