Primary Device ID | 00813250017069 |
NIH Device Record Key | c7c30652-38d4-40ac-acd1-1bdafe6dcce1 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | RFK21-54-5CS |
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 | 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 Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00813250017069 [Package] Contains: 00813250017076 Package: [10 Units] In Commercial Distribution |
GS1 | 00813250017076 [Primary] |
GXD | GENERATOR, LESION, RADIOFREQUENCY |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-10-08 |
Device Publish Date | 2017-06-29 |
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