NIM CONTACT®
GUDID 00643169358751
ENDOTRACH TUBE 8229506 CONT EMG 6MM ROHS
MEDTRONIC XOMED, INC.
Basic endotracheal tube, single-use Basic endotracheal tube, single-use Basic endotracheal tube, single-use Basic endotracheal tube, single-use Basic endotracheal tube, single-use Basic endotracheal tube, single-use Basic endotracheal tube, single-use Basic endotracheal tube, single-use Basic endotracheal tube, single-use Basic endotracheal tube, single-use Basic endotracheal tube, single-use Basic endotracheal tube, single-use Basic endotracheal tube, single-use Basic endotracheal tube, single-use Basic endotracheal tube, single-use Basic endotracheal tube, single-use Basic endotracheal tube, single-use Basic endotracheal tube, single-use Basic endotracheal tube, single-use Basic endotracheal tube, single-use Basic endotracheal tube, single-use Basic endotracheal tube, single-use Basic endotracheal tube, single-use Basic endotracheal tube, single-use Basic endotracheal tube, single-use Basic endotracheal tube, single-use| Primary Device ID | 00643169358751 |
| NIH Device Record Key | 7e3c34e4-748e-4eee-8e87-80677682ab77 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NIM CONTACT® |
| Version Model Number | 8229506 |
| Company DUNS | 835465063 |
| Company Name | MEDTRONIC XOMED, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| 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 | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
Device Dimensions
| Outer Diameter | 9 Millimeter |
| Outer Diameter | 9 Millimeter |
| Outer Diameter | 9 Millimeter |
| Outer Diameter | 9 Millimeter |
| Lumen/Inner Diameter | 6 Millimeter |
| Outer Diameter | 9 Millimeter |
| Lumen/Inner Diameter | 6 Millimeter |
| Outer Diameter | 9 Millimeter |
| Lumen/Inner Diameter | 6 Millimeter |
| Outer Diameter | 9 Millimeter |
| Lumen/Inner Diameter | 6 Millimeter |
| Outer Diameter | 9 Millimeter |
| Lumen/Inner Diameter | 6 Millimeter |
| Outer Diameter | 9 Millimeter |
| Lumen/Inner Diameter | 6 Millimeter |
| Outer Diameter | 9 Millimeter |
| Lumen/Inner Diameter | 6 Millimeter |
| Outer Diameter | 9 Millimeter |
| Lumen/Inner Diameter | 6 Millimeter |
| Outer Diameter | 9 Millimeter |
| Lumen/Inner Diameter | 6 Millimeter |
| Outer Diameter | 9 Millimeter |
| Lumen/Inner Diameter | 6 Millimeter |
| Outer Diameter | 9 Millimeter |
| Lumen/Inner Diameter | 6 Millimeter |
| Outer Diameter | 9 Millimeter |
| Lumen/Inner Diameter | 6 Millimeter |
| Outer Diameter | 9 Millimeter |
| Lumen/Inner Diameter | 6 Millimeter |
| Outer Diameter | 9 Millimeter |
| Lumen/Inner Diameter | 6 Millimeter |
| Outer Diameter | 9 Millimeter |
| Lumen/Inner Diameter | 6 Millimeter |
| Outer Diameter | 9 Millimeter |
| Lumen/Inner Diameter | 6 Millimeter |
| Outer Diameter | 9 Millimeter |
| Lumen/Inner Diameter | 6 Millimeter |
| Outer Diameter | 9 Millimeter |
| Lumen/Inner Diameter | 6 Millimeter |
| Outer Diameter | 9 Millimeter |
| Lumen/Inner Diameter | 6 Millimeter |
| Outer Diameter | 9 Millimeter |
| Lumen/Inner Diameter | 6 Millimeter |
| Outer Diameter | 9 Millimeter |
| Lumen/Inner Diameter | 6 Millimeter |
| Outer Diameter | 9 Millimeter |
| Lumen/Inner Diameter | 6 Millimeter |
| Outer Diameter | 9 Millimeter |
| Lumen/Inner Diameter | 6 Millimeter |
| Outer Diameter | 9 Millimeter |
| Lumen/Inner Diameter | 6 Millimeter |
| Outer Diameter | 9 Millimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00643169358751 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K925640
FDA Product Code
| ETN | STIMULATOR, NERVE |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-04-07 |
On-Brand Devices [NIM CONTACT®]
| 00643169789579 | EMG TUBE 8229508 NIM CONT 8MM ROHS |
| 00643169789562 | EMG TUBE 8229507 NIM CONT 7MM ROHS |
| 00643169789555 | EMG TUBE 8229506 NIM CONT 6MM ROHS |
| 00643169358775 | ENDOTRACH TUBE 8229508 CONT EMG 8MM ROHS |
| 00643169358768 | ENDOTRACH TUBE 8229507 CONT EMG 7MM ROHS |
| 00643169358751 | ENDOTRACH TUBE 8229506 CONT EMG 6MM ROHS |
Trademark Results [NIM CONTACT]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 NIM CONTACT 78600100 3276757 Live/Registered |
Medtronic Xomed, Inc. 2005-04-01 |
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