Saw Blades OSB-LS

GUDID 00842188124853

Saw Blade Oscillating, Long, S-type

TRIMED, INCORPORATED

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 Surgical saw blade, sagittal, single-use Surgical saw blade, sagittal, single-use
Primary Device ID00842188124853
NIH Device Record Key4a0feec2-38d8-4d18-9508-af640f53b978
Commercial Distribution StatusIn Commercial Distribution
Brand NameSaw Blades
Version Model NumberOSB-LS
Catalog NumberOSB-LS
Company DUNS138041277
Company NameTRIMED, INCORPORATED
Device Count1
DM Exempttrue
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 Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(661)255-7406
Emailinfo@trimedortho.com
Phone+1(661)255-7406
Emailinfo@trimedortho.com
Phone+1(661)255-7406
Emailinfo@trimedortho.com
Phone+1(661)255-7406
Emailinfo@trimedortho.com
Phone+1(661)255-7406
Emailinfo@trimedortho.com
Phone+1(661)255-7406
Emailinfo@trimedortho.com
Phone+1(661)255-7406
Emailinfo@trimedortho.com
Phone+1(661)255-7406
Emailinfo@trimedortho.com
Phone+1(661)255-7406
Emailinfo@trimedortho.com
Phone+1(661)255-7406
Emailinfo@trimedortho.com
Phone+1(661)255-7406
Emailinfo@trimedortho.com
Phone+1(661)255-7406
Emailinfo@trimedortho.com
Phone+1(661)255-7406
Emailinfo@trimedortho.com
Phone+1(661)255-7406
Emailinfo@trimedortho.com
Phone+1(661)255-7406
Emailinfo@trimedortho.com
Phone+1(661)255-7406
Emailinfo@trimedortho.com
Phone+1(661)255-7406
Emailinfo@trimedortho.com
Phone+1(661)255-7406
Emailinfo@trimedortho.com
Phone+1(661)255-7406
Emailinfo@trimedortho.com
Phone+1(661)255-7406
Emailinfo@trimedortho.com
Phone+1(661)255-7406
Emailinfo@trimedortho.com
Phone+1(661)255-7406
Emailinfo@trimedortho.com
Phone+1(661)255-7406
Emailinfo@trimedortho.com
Phone+1(661)255-7406
Emailinfo@trimedortho.com
Phone+1(661)255-7406
Emailinfo@trimedortho.com
Phone+1(661)255-7406
Emailinfo@trimedortho.com
Phone+1(661)255-7406
Emailinfo@trimedortho.com
Phone+1(661)255-7406
Emailinfo@trimedortho.com
Phone+1(661)255-7406
Emailinfo@trimedortho.com
Phone+1(661)255-7406
Emailinfo@trimedortho.com
Phone+1(661)255-7406
Emailinfo@trimedortho.com
Phone+1(661)255-7406
Emailinfo@trimedortho.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100842188124853 [Primary]

FDA Product Code

GFABLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00842188124853]

Moist Heat or Steam Sterilization


[00842188124853]

Moist Heat or Steam Sterilization


[00842188124853]

Moist Heat or Steam Sterilization


[00842188124853]

Moist Heat or Steam Sterilization


[00842188124853]

Moist Heat or Steam Sterilization


[00842188124853]

Moist Heat or Steam Sterilization


[00842188124853]

Moist Heat or Steam Sterilization


[00842188124853]

Moist Heat or Steam Sterilization


[00842188124853]

Moist Heat or Steam Sterilization


[00842188124853]

Moist Heat or Steam Sterilization


[00842188124853]

Moist Heat or Steam Sterilization


[00842188124853]

Moist Heat or Steam Sterilization


[00842188124853]

Moist Heat or Steam Sterilization


[00842188124853]

Moist Heat or Steam Sterilization


[00842188124853]

Moist Heat or Steam Sterilization


[00842188124853]

Moist Heat or Steam Sterilization


[00842188124853]

Moist Heat or Steam Sterilization


[00842188124853]

Moist Heat or Steam Sterilization


[00842188124853]

Moist Heat or Steam Sterilization


[00842188124853]

Moist Heat or Steam Sterilization


[00842188124853]

Moist Heat or Steam Sterilization


[00842188124853]

Moist Heat or Steam Sterilization


[00842188124853]

Moist Heat or Steam Sterilization


[00842188124853]

Moist Heat or Steam Sterilization


[00842188124853]

Moist Heat or Steam Sterilization


[00842188124853]

Moist Heat or Steam Sterilization


[00842188124853]

Moist Heat or Steam Sterilization


[00842188124853]

Moist Heat or Steam Sterilization


[00842188124853]

Moist Heat or Steam Sterilization


[00842188124853]

Moist Heat or Steam Sterilization


[00842188124853]

Moist Heat or Steam Sterilization


[00842188124853]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-02-23
Device Publish Date2022-02-15

On-Brand Devices [Saw Blades]

00842188109959Saw Blade Oscillating, 9mm, S-type
00842188109942Saw Blade Oscillating, 9mm, M-type
00842188124860Saw Blade Oscillating, Long, M-type
00842188124853Saw Blade Oscillating, Long, S-type

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