Primary Device ID | 00763000004996 |
NIH Device Record Key | 49ad5319-3df8-46fb-8fc8-cff0e89613fa |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | SR-6000 |
Company DUNS | 796986144 |
Company Name | MEDTRONIC, INC. |
Device Count | 6 |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00763000004996 [Primary] |
GS1 | 70763000004995 [Unit of Use] |
GXR | COVER, BURR HOLE |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-05-21 |
Device Publish Date | 2019-05-13 |
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