I-promelt 39001010

GUDID 04260580283996

Powder, 5kg

S & S Scheftner GmbH

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Primary Device ID04260580283996
NIH Device Record Key09834d1a-a493-4eb7-85a5-8dc839098d40
Commercial Distribution StatusIn Commercial Distribution
Brand NameI-promelt
Version Model Number39001010
Catalog Number39001010
Company DUNS321810517
Company NameS & S Scheftner GmbH
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 Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS104260580283996 [Primary]

FDA Product Code

EJHAlloy, Metal, Base

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-05-16
Device Publish Date2022-05-08

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