Primary Device ID | 10673978521869 |
NIH Device Record Key | 19b67c1b-51e2-4416-8211-86e618308b04 |
Commercial Distribution Discontinuation | 2017-11-29 |
Commercial Distribution Status | Not 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 | 00673978521862 [Primary] |
GS1 | 10673978521869 [Package] Contains: 00673978521862 Package: PK [6 Units] Discontinued: 2017-11-29 Not 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 | 2016-06-30 |
00199150008643 - NA | 2025-05-12 CUSTOM PACK BB5X98R22 UCLA PED |
20199150011609 - NA | 2025-05-12 CUSTOM PACK 12P80R 20PK 1/2 X 3/8 CONN L |
00199150011612 - NA | 2025-05-12 CUSTOM PACK BB11U88R7 PEDI ADAPTATI |
00199150011629 - NA | 2025-05-12 CUSTOM PACK BB3F83R10 HEAD PK |
00199150014361 - NA | 2025-05-12 CUSTOM PACK BB7X79R6 CP PRIME |
20199150014594 - NA | 2025-05-12 CUSTOM PACK BB8Q15R2 10PK 1/2 VENOUS |
00199150014606 - NA | 2025-05-12 CUSTOM PACK BB10M30R1 OXY EXCHANGE |
00199150014613 - NA | 2025-05-12 CUSTOM PACK BB10Y54R5 ECC PED 1/4 |