NIM-2®
GUDID 20681490176662
HANDLE 8225051 10PK MONOPOLAR PROBE ROHS
MEDTRONIC XOMED, INC.
Nerve-locating system, line-powered| Primary Device ID | 20681490176662 |
| NIH Device Record Key | 0268d257-e408-4591-8991-acc2d96554fe |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NIM-2® |
| Version Model Number | 8225051 |
| 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 |
Customer Support Contacts
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00681490176668 [Primary] |
| GS1 | 20681490176662 [Package] Contains: 00681490176668 Package: PK [10 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K934426
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 | 2016-04-17 |
On-Brand Devices [NIM-2®]
| 20681490176662 | HANDLE 8225051 10PK MONOPOLAR PROBE ROHS |
| 20763000040707 | HANDLE 8225051 10PK MONOPOLAR PROBE ROHS |
Trademark Results [NIM-2]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 NIM-2 74247770 1727352 Dead/Cancelled |
MEDTRONIC XOMED, INC. 1992-02-20 |
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