Primary Device ID | 10381780505631 |
NIH Device Record Key | fa9c9020-f42d-453a-9dd3-7967a63053f3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Panta® 2 |
Version Model Number | PAN-1010-0185 |
Catalog Number | PAN-1010-0185 |
Company DUNS | 942377524 |
Company Name | Ascension Orthopedics, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
Special Storage Condition, Specify | Between 0 and 0 *Do Not Use if Package is Damaged |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10381780505631 [Primary] |
LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
Steralize Prior To Use | true |
Device Is Sterile | false |
[10381780505631]
Moist Heat or Steam Sterilization
[10381780505631]
Moist Heat or Steam Sterilization
[10381780505631]
Moist Heat or Steam Sterilization
[10381780505631]
Moist Heat or Steam Sterilization
[10381780505631]
Moist Heat or Steam Sterilization
[10381780505631]
Moist Heat or Steam Sterilization
[10381780505631]
Moist Heat or Steam Sterilization
[10381780505631]
Moist Heat or Steam Sterilization
[10381780505631]
Moist Heat or Steam Sterilization
[10381780505631]
Moist Heat or Steam Sterilization
[10381780505631]
Moist Heat or Steam Sterilization
[10381780505631]
Moist Heat or Steam Sterilization
[10381780505631]
Moist Heat or Steam Sterilization
[10381780505631]
Moist Heat or Steam Sterilization
[10381780505631]
Moist Heat or Steam Sterilization
[10381780505631]
Moist Heat or Steam Sterilization
[10381780505631]
Moist Heat or Steam Sterilization
[10381780505631]
Moist Heat or Steam Sterilization
[10381780505631]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2020-04-06 |
Device Publish Date | 2018-11-13 |
10381780505648 | Arthrodesis Nail System Drill Guide, ø4.1mm, Tibial |
10381780505631 | Arthrodesis Nail System Drill Guide, ø4.1mm, Calcaneal |
10381780505624 | Arthrodesis Nail System Soft Tissue Protector, ø7mm, Tibia |
10381780505617 | Arthrodesis Nail System Soft Tissue Protector, ø7mm, Calcaneal |
10381780505600 | Arthrodesis Nail System Compression Rod Drill Guide, ø5mm |
10381780505495 | Arthrodesis Nail System External Protection Sleeve ø13.5mm |
10381780505488 | Arthrodesis Nail System Central Protection Sleeve ø9mm |
10381780505471 | Arthrodesis Nail System Internal Protection Sleeve ø3.2mm |
10381780505808 | Arthrodesis Nail System Tibial Drill, ø4.1mm |
10381780505792 | Arthrodesis Nail System Long Calcaneal Drill, ø4.1mm |
10381780505785 | Arthrodesis Nail System Short Calcaneal Drill, ø4.1mm |
10381780505365 | Arthrodesis Nail System End Cap |
10381780505372 | Arthrodesis Nail System End Cap |
10381780505839 | Arthrodesis Nail System Screw Caddy Lid |
10381780505761 | Arthrodesis Nail System Screw Case Lid |
10381780505754 | Arthrodesis Nail System Screw Case |
10381780505747 | Arthrodesis Nail System Panta 2 Lid |
10381780505730 | Arthrodesis Nail System Targeting Guide Tray |
10381780505723 | Arthrodesis Nail System Targeting Guide and Compression Device Case |
10381780505716 | Arthrodesis Nail System Nail and Screw Prep Case |
10381780505709 | Arthrodesis Nail System Screw Caddy |
10381780504450 | Arthrodesis Nail System Nail, ø13mm X 240mm |
10381780504443 | Arthrodesis Nail System Nail, ø13mm X 210mm |
10381780504436 | Arthrodesis Nail System Nail, ø13mm X 180mm |
10381780504429 | Arthrodesis Nail System Nail, ø13mm X 150mm |
10381780504412 | Arthrodesis Nail System Nail, ø12mm X 240mm |
10381780504405 | Arthrodesis Nail System Nail, ø12mm X 210mm |
10381780504399 | Arthrodesis Nail System Nail, ø12mm X 180mm |
10381780504382 | Arthrodesis Nail System Nail, ø12mm X 150mm |
10381780504375 | Arthrodesis Nail System Nail, ø11mm X 240mm |
10381780504368 | Arthrodesis Nail System Nail, ø11mm X 210mm |
10381780504351 | Arthrodesis Nail System Nail, ø11mm X 180mm |
10381780504344 | Arthrodesis Nail System Nail, ø11mm X 150mm |
10381780504337 | Arthrodesis Nail System Nail, ø10mm X 240mm |
10381780504320 | Arthrodesis Nail System Nail, ø10mm X 210mm |
10381780504313 | Arthrodesis Nail System Nail, ø10mm X 180mm |
10381780504306 | Arthrodesis Nail System Nail, ø10mm X 150mm |
10381780505778 | Arthrodesis Nail System T-Handle with AO Quick Connect |
10381780505822 | Arthrodesis Nail System Cannulated Drill ø9mm x 185mm |
10381780505815 | Arthrodesis Nail System Cannulated Drill ø7mm x 185mm |
10381780505693 | Arthrodesis Nail System K-Wire, ø2.5mm x 150mm |
10381780505686 | Arthrodesis Nail System Target Guide Support |
10381780505679 | Arthrodesis Nail System AO Driver Shaft - 3.5mm Hex Screwdriver, Self-Retaining |
10381780505662 | Arthrodesis Nail System 4.1mm Trocar |
10381780505655 | Arthrodesis Nail System Tissue Protector Removal Tool |
10381780505594 | Arthrodesis Nail System Compression Rod, ø5mm |
10381780505587 | Arthrodesis Nail System Depth gauge |
10381780505570 | Arthrodesis Nail System Compression Wheel |
10381780505563 | Arthrodesis Nail System Compression Device |
10381780505556 | Arthrodesis Nail System Lock Screw |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PANTA 97180364 not registered Live/Pending |
Iris Restaurant Group 2021-12-20 |
PANTA 88776510 not registered Live/Pending |
VIP Products L.L.C. 2020-01-28 |
PANTA 88548512 not registered Live/Pending |
NINGBO XINMAI EXHIBITION EQUIPMENT CO.,LTD 2019-07-30 |
PANTA 85006649 4152440 Live/Registered |
Sumida flexible connections GmbH 2010-04-05 |
PANTA 79230375 not registered Live/Pending |
PANTAFLIX AG 2017-09-13 |
PANTA 79018294 3168990 Live/Registered |
NEWDEAL 2005-09-26 |
PANTA 78485363 3160179 Dead/Cancelled |
Panta Systems, Inc. 2004-09-17 |
PANTA 78485355 3130908 Dead/Cancelled |
Panta Systems, Inc. 2004-09-17 |
PANTA 73567136 1476904 Dead/Cancelled |
PANTASHOP 1985-11-06 |