CMP-02795

GUDID 00840200409766

T25 Tapered Driver - 1/4 Square

Integrity Implants Inc.

Surgical screwdriver, reusable
Primary Device ID00840200409766
NIH Device Record Keyf1961ed6-0b5c-4f5b-8e3d-98da6137b825
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberCMP-02795
Catalog NumberCMP-02795
Company DUNS080300717
Company NameIntegrity Implants Inc.
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 Usefalse
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

Customer Support Contacts

Phone800.201.9300
Emailcustomerservice@integrityimplants.com
Phone800.201.9300
Emailcustomerservice@integrityimplants.com
Phone800.201.9300
Emailcustomerservice@integrityimplants.com
Phone800.201.9300
Emailcustomerservice@integrityimplants.com
Phone800.201.9300
Emailcustomerservice@integrityimplants.com
Phone800.201.9300
Emailcustomerservice@integrityimplants.com
Phone800.201.9300
Emailcustomerservice@integrityimplants.com
Phone800.201.9300
Emailcustomerservice@integrityimplants.com
Phone800.201.9300
Emailcustomerservice@integrityimplants.com
Phone800.201.9300
Emailcustomerservice@integrityimplants.com
Phone800.201.9300
Emailcustomerservice@integrityimplants.com
Phone800.201.9300
Emailcustomerservice@integrityimplants.com
Phone800.201.9300
Emailcustomerservice@integrityimplants.com
Phone800.201.9300
Emailcustomerservice@integrityimplants.com
Phone800.201.9300
Emailcustomerservice@integrityimplants.com
Phone800.201.9300
Emailcustomerservice@integrityimplants.com
Phone800.201.9300
Emailcustomerservice@integrityimplants.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100840200409766 [Primary]

FDA Product Code

HXXScrewdriver

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00840200409766]

Moist Heat or Steam Sterilization


[00840200409766]

Moist Heat or Steam Sterilization


[00840200409766]

Moist Heat or Steam Sterilization


[00840200409766]

Moist Heat or Steam Sterilization


[00840200409766]

Moist Heat or Steam Sterilization


[00840200409766]

Moist Heat or Steam Sterilization


[00840200409766]

Moist Heat or Steam Sterilization


[00840200409766]

Moist Heat or Steam Sterilization


[00840200409766]

Moist Heat or Steam Sterilization


[00840200409766]

Moist Heat or Steam Sterilization


[00840200409766]

Moist Heat or Steam Sterilization


[00840200409766]

Moist Heat or Steam Sterilization


[00840200409766]

Moist Heat or Steam Sterilization


[00840200409766]

Moist Heat or Steam Sterilization


[00840200409766]

Moist Heat or Steam Sterilization


[00840200409766]

Moist Heat or Steam Sterilization


[00840200409766]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-02-01
Device Publish Date2024-01-24

Devices Manufactured by Integrity Implants Inc.

00840200410229 - NA2024-10-28 5.5-6.0 MIS Counter Torque - No Lip
00840200402477 - LineSider2024-10-25 5.5/6.0mm, Non-mod Standard 7.1mm- Iliac Shank - 9.5mm x 90mm
00840200407373 - N/A2024-10-25 Open Disc Prep Insert 2
00840200405492 - NA2024-09-09 BH Tapered Screw Starter
00840200410045 - N/A2024-07-18 SS Right Blade, 80mm
00840200410052 - N/A2024-07-18 SS Right Blade, 70mm
00840200410069 - N/A2024-07-18 SS Right Blade, 60mm
00840200410076 - N/A2024-07-18 SS Right Blade, 50mm

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