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 |