Primary Device ID | 00613994520456 |
NIH Device Record Key | 30085eaa-1c0a-4d67-81fa-81c59c6de6c5 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | ATL2001 |
Company DUNS | 006261481 |
Company Name | MEDTRONIC, INC. |
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 | true |
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 | 00613994520456 [Primary] |
GS1 | 20613994520450 [Package] Package: PK [6 Units] In Commercial Distribution |
CAC | APPARATUS, AUTOTRANSFUSION |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-06-09 |
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