Primary Device ID | 00813250010107 |
NIH Device Record Key | 0d5a1e4e-31f0-4ba2-ba7b-71c87b943ec8 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | CSK-TC10 |
Company DUNS | 824951958 |
Company Name | BOSTON SCIENTIFIC NEUROMODULATION CORPORATION |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00813250010107 [Primary] |
GXI | PROBE, RADIOFREQUENCY LESION |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00813250010107]
Moist Heat or Steam Sterilization
[00813250010107]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-10-08 |
Device Publish Date | 2017-08-21 |
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