Wedge 3 MBUR2913

GUDID 14053613287484

Gebr. Brasseler GmbH & Co. KG

Orthopaedic bur, single-use
Primary Device ID14053613287484
NIH Device Record Key1337f626-cd41-4899-b13a-8c69e26b7ec5
Commercial Distribution StatusIn Commercial Distribution
Brand NameWedge 3
Version Model NumberMBUR2913
Catalog NumberMBUR2913
Company DUNS317409001
Company NameGebr. Brasseler GmbH & Co. KG
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 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
GS114053613287484 [Primary]

FDA Product Code

GFFBur, Surgical, General & Plastic Surgery

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-04-25
Device Publish Date2024-04-17

On-Brand Devices [Wedge 3]

24053613288419DW311065R-S
14053613287484MBUR2913
24053613288365P65-108-2913-S
14053613291214TM22913
14053613291207TM12913

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.