KOMET STEINMANN PIN SP001.300.032 STE

GUDID 24053613285586

Gebr. Brasseler GmbH & Co. KG

Orthopaedic bone pin, non-bioabsorbable
Primary Device ID24053613285586
NIH Device Record Key73dc85df-0d56-401a-8ecc-405eb96def4e
Commercial Distribution StatusIn Commercial Distribution
Brand NameKOMET STEINMANN PIN
Version Model NumberSP001.300.032.M1
Catalog NumberSP001.300.032 STE
Company DUNS317409001
Company NameGebr. Brasseler GmbH & Co. KG
Device Count1
DM Exempttrue
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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS114053613285589 [Primary]
GS124053613285586 [Package]
Contains: 14053613285589
Package: [1 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HTYPin, Fixation, Smooth

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2023-09-18
Device Publish Date2023-01-12

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E226046068TW0804-07-338
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84053613161486SP004.228.040.K4
84053613160656SP002.228.024.K4
84053613160632SP002.228.020.K4
84053613160489SP002.152.020.K4
84053613159964SP001.228.024.k4
84053613159940SP001.228.020.K4
84053613159926SP001.152.048.K4
84053613159865SP001.152.032.K4
84053613159247SP003.228.024.K4
84053613156918SP002.152.016.K4
84053613155911SP001.152.016.K4
84053613161240SP001.152.020.K4
84053613159827SP001.152.024.K4
84053613156413SP004.152.016.K4
84053613160670SP002.228.028.K4
84053613155812SP001.127.016.K4
24053613285586SP001.300.032.M1

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