Primary Device ID | 10850040767008 |
NIH Device Record Key | f36c9c6c-b545-4969-9c0e-484a4f6e9cda |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Nimbus |
Version Model Number | NIM-100-10BB |
Company DUNS | 117402924 |
Company Name | Stratus Medical LLC |
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 | 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 | 00850040767001 [Primary] |
GS1 | 10850040767008 [Package] Contains: 00850040767001 Package: [10 Units] In Commercial Distribution |
GXI | Probe, Radiofrequency Lesion |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-09-20 |
Device Publish Date | 2022-09-12 |
10850040767039 | Electrosurgical RF Multitined Expandable Electrode |
10850040767022 | Electrosurgical RF Multitined Expandable Electrode |
10850040767015 | Electrosurgical RF Multitined Expandable Electrode |
10850040767008 | Electrosurgical RF Multitined Expandable Electrode |