Primary Device ID | 10817489025205 |
NIH Device Record Key | 3c18f715-130c-498d-a905-5f4973e5773b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Spetzler™ Lighted Suction Tube, 3 French, 120mm long |
Version Model Number | DN1503-120 |
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 | 00817489025208 [Unit of Use] |
GS1 | 10817489025205 [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 | 5 |
Public Version Date | 2020-04-20 |
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 |