| Primary Device ID | 10817489025243 |
| NIH Device Record Key | dd0205b2-7b47-4e9e-9b94-2a0398e1e4eb |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Spetzler™ Lighted Suction Tube, 5 French, 140mm long |
| Version Model Number | DN1505-140 |
| Company DUNS | 007883297 |
| Company Name | KATALYST SURGICAL LLC |
| Device Count | 5 |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00817489025246 [Unit of Use] |
| GS1 | 10817489025243 [Primary] |
| FST | Light, Surgical, Fiberoptic |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-05-07 |
| Device Publish Date | 2017-08-09 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SPETZLER 77726480 not registered Dead/Abandoned |
Spetzler, Robert F. 2009-04-30 |
![]() SPETZLER 75563950 not registered Dead/Abandoned |
Robert F. Spetzler, M.D. 1998-10-02 |
![]() SPETZLER 73408581 1350488 Dead/Cancelled |
AMERICAN HOSPITAL SUPPLY CORPORATION 1983-01-07 |