| Primary Device ID | 00846159028843 |
| NIH Device Record Key | 5a6b8859-6ae5-41a3-8fc7-6b6c89cff3f7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SCANLAN Minimally-Invasive Instrumentation |
| Version Model Number | 9909-914 |
| Catalog Number | 9909-914 |
| Company DUNS | 023055619 |
| Company Name | SCANLAN INTERNATIONAL INC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 | 651-297-0997 |
| vanderpoelw@scanlangroup.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00846159028843 [Primary] |
| GCJ | Laparoscope, General & Plastic Surgery |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00846159028843]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-12-02 |
| Device Publish Date | 2019-11-22 |
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