| Primary Device ID | 00681490069281 |
| NIH Device Record Key | 80c09759-2ebb-4531-9c3b-9155b8af88e9 |
| Commercial Distribution Discontinuation | 2018-10-24 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Micro-Craft® |
| Version Model Number | 3118505 |
| Company DUNS | 835465063 |
| Company Name | MEDTRONIC XOMED, 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 | true |
| 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 | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00681490069281 [Primary] |
| ERL | DRILL, SURGICAL, ENT (ELECTRIC OR PNEUMATIC) INCLUDING HANDPIECE |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 6 |
| Public Version Date | 2019-04-23 |
| Device Publish Date | 2016-04-29 |
| 00681490069281 | TUBING 3118505 MICROCRAFT IRRIGATION |
| 00763000040611 | BUR 3112964C 5PK 3MM 64MM L ROUND SST |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MICRO-CRAFT 74054114 1634196 Dead/Cancelled |
Queen Carpet Corporation 1990-04-30 |
![]() MICRO-CRAFT 73263038 1164535 Dead/Cancelled |
XOMED INC. 1980-05-21 |