Primary Device ID | 15060391210350 |
NIH Device Record Key | de43361f-5e9a-4f29-b105-619d5755fbb2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sentimag |
Version Model Number | Gen 3 Thin Probe |
Catalog Number | SMP03T |
Company DUNS | 846963171 |
Company Name | ENDOMAGNETICS LTD |
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 | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 15060391210350 [Primary] |
PUV | Lymph Node Location System During Sentinel Biopsy Procedure |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2024-03-22 |
Device Publish Date | 2024-02-09 |
15060391210350 | Thin Probe for Sentimag Gen 3 |
15060391210312 | Sentimag Gen 3 Base Unit |
15060391210343 | Probe checker for Sentimag Gen 3 Probe |
15060391210336 | Footswitch for Sentimag Gen 3 |
15060391210329 | Standard Probe for Sentimag Gen 3 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SENTIMAG 77885534 4173357 Live/Registered |
Endomagnetics Limited 2009-12-03 |