Saw Blade for Stryker® P65-151-P300-S

GUDID 24053613289379

Gebr. Brasseler GmbH & Co. KG

Surgical saw blade, sagittal, single-use Surgical saw blade, sagittal, single-use Surgical saw blade, sagittal, single-use Surgical saw blade, sagittal, single-use Surgical saw blade, sagittal, single-use Surgical saw blade, sagittal, single-use Surgical saw blade, sagittal, single-use Surgical saw blade, sagittal, single-use Surgical saw blade, sagittal, single-use Surgical saw blade, sagittal, single-use Surgical saw blade, sagittal, single-use Surgical saw blade, sagittal, single-use Surgical saw blade, sagittal, single-use Surgical saw blade, sagittal, single-use Surgical saw blade, sagittal, single-use Surgical saw blade, sagittal, single-use Surgical saw blade, sagittal, single-use Surgical saw blade, sagittal, single-use Surgical saw blade, sagittal, single-use Surgical saw blade, sagittal, single-use Surgical saw blade, sagittal, single-use Surgical saw blade, sagittal, single-use Surgical saw blade, sagittal, single-use Surgical saw blade, sagittal, single-use Surgical saw blade, sagittal, single-use Surgical saw blade, sagittal, single-use Surgical saw blade, sagittal, single-use Surgical saw blade, sagittal, single-use Surgical saw blade, sagittal, single-use Surgical saw blade, sagittal, single-use
Primary Device ID24053613289379
NIH Device Record Key385a114c-8598-49bf-9a4a-17e2b343ef19
Commercial Distribution StatusIn Commercial Distribution
Brand NameSaw Blade for Stryker®
Version Model NumberP65-151-P300-S
Catalog NumberP65-151-P300-S
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
GS114053613289372 [Primary]
GS124053613289379 [Package]
Contains: 14053613289372
Package: [1 Units]
In Commercial Distribution

FDA Product Code

GFABlade, Saw, General & Plastic Surgery, Surgical

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-02-29
Device Publish Date2024-02-21

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