ASY-01109

GUDID 00840200409421

Graft Tamp XL

Integrity Implants Inc.

Surgical tamp, reusable
Primary Device ID00840200409421
NIH Device Record Key15240b81-3c2f-4ec3-add2-8c8a9925d493
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberASY-01109
Catalog NumberASY-01109
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

Phone8002019300
Emailcustomerservice@integrityimplants.com
Phone8002019300
Emailcustomerservice@integrityimplants.com
Phone8002019300
Emailcustomerservice@integrityimplants.com
Phone8002019300
Emailcustomerservice@integrityimplants.com
Phone8002019300
Emailcustomerservice@integrityimplants.com
Phone8002019300
Emailcustomerservice@integrityimplants.com
Phone8002019300
Emailcustomerservice@integrityimplants.com
Phone8002019300
Emailcustomerservice@integrityimplants.com
Phone8002019300
Emailcustomerservice@integrityimplants.com
Phone8002019300
Emailcustomerservice@integrityimplants.com
Phone8002019300
Emailcustomerservice@integrityimplants.com
Phone8002019300
Emailcustomerservice@integrityimplants.com
Phone8002019300
Emailcustomerservice@integrityimplants.com
Phone8002019300
Emailcustomerservice@integrityimplants.com
Phone8002019300
Emailcustomerservice@integrityimplants.com
Phone8002019300
Emailcustomerservice@integrityimplants.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100840200409421 [Primary]

FDA Product Code

LXHOrthopedic Manual Surgical Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00840200409421]

Moist Heat or Steam Sterilization


[00840200409421]

Moist Heat or Steam Sterilization


[00840200409421]

Moist Heat or Steam Sterilization


[00840200409421]

Moist Heat or Steam Sterilization


[00840200409421]

Moist Heat or Steam Sterilization


[00840200409421]

Moist Heat or Steam Sterilization


[00840200409421]

Moist Heat or Steam Sterilization


[00840200409421]

Moist Heat or Steam Sterilization


[00840200409421]

Moist Heat or Steam Sterilization


[00840200409421]

Moist Heat or Steam Sterilization


[00840200409421]

Moist Heat or Steam Sterilization


[00840200409421]

Moist Heat or Steam Sterilization


[00840200409421]

Moist Heat or Steam Sterilization


[00840200409421]

Moist Heat or Steam Sterilization


[00840200409421]

Moist Heat or Steam Sterilization


[00840200409421]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-06-21
Device Publish Date2023-06-13

Devices Manufactured by Integrity Implants Inc.

00840200409780 - NA2025-04-16 Adjustable Depth Stop, Tall, FH7 MIS2
00840200409797 - N/A2025-04-16 Short Cannula Body, FH7 MIS2
00840200409803 - N/A2025-04-16 Tall Cannula Body, FH7 MIS2
00840200409827 - NA2025-04-16 Dilator Handle, FH7 MIS2
00840200409858 - N/A2025-04-16 Articulating Curette, FH7 MIS2
00840200409872 - NA2025-04-16 7mm Open Shaver, FH7 MIS2
00840200409889 - NA2025-04-16 8mm Open Shaver, FH7 MIS2
00840200409896 - NA2025-04-16 9mm Open Shaver, FH7 MIS2

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