SCANLAN® Tunneler Instrumentation COA016-09
GUDID 00846159035995
SCANLAN® A/V Access Tunneler
SCANLAN INTERNATIONAL INC
Vascular graft tunneller| Primary Device ID | 00846159035995 |
| NIH Device Record Key | bf455ed5-3659-40fe-a1c3-1259a5f75b2e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SCANLAN® Tunneler Instrumentation |
| Version Model Number | COA016-09 |
| Catalog Number | COA016-09 |
| 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 |
Customer Support Contacts
| 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00846159035995 [Primary] |
FDA Product Code
| DWS | Instruments, Surgical, Cardiovascular |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00846159035995]
Moist Heat or Steam Sterilization
[00846159035995]
Moist Heat or Steam Sterilization
[00846159035995]
Moist Heat or Steam Sterilization
[00846159035995]
Moist Heat or Steam Sterilization
[00846159035995]
Moist Heat or Steam Sterilization
[00846159035995]
Moist Heat or Steam Sterilization
[00846159035995]
Moist Heat or Steam Sterilization
[00846159035995]
Moist Heat or Steam Sterilization
[00846159035995]
Moist Heat or Steam Sterilization
[00846159035995]
Moist Heat or Steam Sterilization
[00846159035995]
Moist Heat or Steam Sterilization
[00846159035995]
Moist Heat or Steam Sterilization
[00846159035995]
Moist Heat or Steam Sterilization
[00846159035995]
Moist Heat or Steam Sterilization
[00846159035995]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-11-21 |
| Device Publish Date | 2022-11-11 |
On-Brand Devices [SCANLAN® Tunneler Instrumentation]
| 00846159035995 | SCANLAN® A/V Access Tunneler |
| 00846159036008 | SCANLAN® A/V Access Tunneler |
Trademark Results [SCANLAN]
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 |
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