Primary Device ID | 00846159026801 |
NIH Device Record Key | 68424ff8-d6df-4a44-af5b-e1b78db4cc5d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SCANLAN® Instrumentation |
Version Model Number | 8008-430-13 |
Catalog Number | 8008-430-13 |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00846159026801 [Primary] |
GZX | Instrument, Microsurgical |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00846159026801]
Moist Heat or Steam Sterilization
[00846159026801]
Moist Heat or Steam Sterilization
[00846159026801]
Moist Heat or Steam Sterilization
[00846159026801]
Moist Heat or Steam Sterilization
[00846159026801]
Moist Heat or Steam Sterilization
[00846159026801]
Moist Heat or Steam Sterilization
[00846159026801]
Moist Heat or Steam Sterilization
[00846159026801]
Moist Heat or Steam Sterilization
[00846159026801]
Moist Heat or Steam Sterilization
[00846159026801]
Moist Heat or Steam Sterilization
[00846159026801]
Moist Heat or Steam Sterilization
[00846159026801]
Moist Heat or Steam Sterilization
[00846159026801]
Moist Heat or Steam Sterilization
[00846159026801]
Moist Heat or Steam Sterilization
[00846159026801]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-06-19 |
Device Publish Date | 2019-06-11 |
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 |