| Primary Device ID | 00846159033229 |
| NIH Device Record Key | 938f593c-0bdf-4b16-bf50-ba4c801932b8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SCANLAN® Neuro Instruments |
| Version Model Number | 3003-841 |
| Catalog Number | 3003-841 |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00846159033229 [Primary] |
| GEN | Forceps, General & Plastic Surgery |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00846159033229]
Moist Heat or Steam Sterilization
[00846159033229]
Moist Heat or Steam Sterilization
[00846159033229]
Moist Heat or Steam Sterilization
[00846159033229]
Moist Heat or Steam Sterilization
[00846159033229]
Moist Heat or Steam Sterilization
[00846159033229]
Moist Heat or Steam Sterilization
[00846159033229]
Moist Heat or Steam Sterilization
[00846159033229]
Moist Heat or Steam Sterilization
[00846159033229]
Moist Heat or Steam Sterilization
[00846159033229]
Moist Heat or Steam Sterilization
[00846159033229]
Moist Heat or Steam Sterilization
[00846159033229]
Moist Heat or Steam Sterilization
[00846159033229]
Moist Heat or Steam Sterilization
[00846159033229]
Moist Heat or Steam Sterilization
[00846159033229]
Moist Heat or Steam Sterilization
[00846159033229]
Moist Heat or Steam Sterilization
[00846159033229]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-06-06 |
| Device Publish Date | 2025-05-29 |
| 00846159012774 | Scanlan Micro Fcp, fh, bayo sty, 45° angle, 0.3mm DD tips, 8-3/4"/22 cm |
| 00846159033229 | Scanlan Micro Fcp, fh, bayo sty, 45° angle, 0.3mm DD tips, 8-3/4"/22 cm |
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 |