| Primary Device ID | 00846159036046 |
| NIH Device Record Key | 06a20999-5c08-4d68-a7ec-918ec4e508bc |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SCANLAN® Instrumentation |
| Version Model Number | 9009-823-16 |
| Catalog Number | 9009-823-16 |
| Company DUNS | 023055619 |
| Company Name | SCANLAN INTERNATIONAL 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 | 651-298-0997 |
| vanderpoelw@scanlangroup.com | |
| Phone | 651-298-0997 |
| vanderpoelw@scanlangroup.com | |
| Phone | 651-298-0997 |
| vanderpoelw@scanlangroup.com | |
| Phone | 651-298-0997 |
| vanderpoelw@scanlangroup.com | |
| Phone | 651-298-0997 |
| vanderpoelw@scanlangroup.com | |
| Phone | 651-298-0997 |
| vanderpoelw@scanlangroup.com | |
| Phone | 651-298-0997 |
| vanderpoelw@scanlangroup.com | |
| Phone | 651-298-0997 |
| vanderpoelw@scanlangroup.com | |
| Phone | 651-298-0997 |
| vanderpoelw@scanlangroup.com | |
| Phone | 651-298-0997 |
| vanderpoelw@scanlangroup.com | |
| Phone | 651-298-0997 |
| vanderpoelw@scanlangroup.com | |
| Phone | 651-298-0997 |
| vanderpoelw@scanlangroup.com | |
| Phone | 651-298-0997 |
| vanderpoelw@scanlangroup.com | |
| Phone | 651-298-0997 |
| vanderpoelw@scanlangroup.com | |
| Phone | 651-298-0997 |
| vanderpoelw@scanlangroup.com | |
| Phone | 651-298-0997 |
| vanderpoelw@scanlangroup.com | |
| Phone | 651-298-0997 |
| vanderpoelw@scanlangroup.com | |
| Phone | 651-298-0997 |
| vanderpoelw@scanlangroup.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00846159036046 [Primary] |
| HTE | Elevator |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00846159036046]
Moist Heat or Steam Sterilization
[00846159036046]
Moist Heat or Steam Sterilization
[00846159036046]
Moist Heat or Steam Sterilization
[00846159036046]
Moist Heat or Steam Sterilization
[00846159036046]
Moist Heat or Steam Sterilization
[00846159036046]
Moist Heat or Steam Sterilization
[00846159036046]
Moist Heat or Steam Sterilization
[00846159036046]
Moist Heat or Steam Sterilization
[00846159036046]
Moist Heat or Steam Sterilization
[00846159036046]
Moist Heat or Steam Sterilization
[00846159036046]
Moist Heat or Steam Sterilization
[00846159036046]
Moist Heat or Steam Sterilization
[00846159036046]
Moist Heat or Steam Sterilization
[00846159036046]
Moist Heat or Steam Sterilization
[00846159036046]
Moist Heat or Steam Sterilization
[00846159036046]
Moist Heat or Steam Sterilization
[00846159036046]
Moist Heat or Steam Sterilization
[00846159036046]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-04-22 |
| Device Publish Date | 2024-04-12 |
| 00846159026801 | SCANLAN® Septal Hook |
| 00846159026764 | SCANLAN® Septal Hook |
| 00846159035643 | SCANLAN® Cardiovascular Probe |
| 00846159033656 | Kerrison Style Wire Cutter |
| 00846159035858 | SCANLAN® Retractor Blade |
| 00846159035841 | SCANLAN® Retractor Blade |
| 00846159035919 | Suction Instrument |
| 00846159036046 | Miller™ Periosteal Elevator Curved |
| 00846159036039 | Miller™ Periosteal Elevator Curved |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SCANLAN 74389302 1837794 Live/Registered |
Scanlan International, Inc. 1993-05-07 |
![]() SCANLAN 73625084 1439873 Live/Registered |
SCANLAN INTERNATIONAL, INC. 1986-10-14 |