Primary Device ID | 10673978522248 |
NIH Device Record Key | cf1c6c69-fe3f-40b1-96f5-30979dd8d822 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | BT133 |
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 | 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 | 00673978522241 [Primary] |
GS1 | 10673978522248 [Package] Contains: 00673978522241 Package: PK [10 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 | 2015-06-17 |
00199150050161 - NA | 2025-09-29 CUSTOM PACK HLO BB12D44R4 PUMP PK |
00199150050178 - NA | 2025-09-29 CUSTOM PACK BB4W67R26 EVL ADULT E |
00199150050185 - NA | 2025-09-29 CUSTOM PACK BB4Q12R27 UNIV H/L |
20199150050202 - NA | 2025-09-29 CUSTOM PACK BB12P63R 4PK GPS TABLE PK |
00199150050871 - NA | 2025-09-29 CUSTOM PACK BB11R66R2 TBL 1/4 |
00763000877033 - SPRINTER® LEGEND | 2025-09-29 BALLOON SPL15006X SPR LEG RX US M |
00763000877040 - SPRINTER® LEGEND | 2025-09-29 BALLOON SPL15010X SPR LEG RX US M |
00763000877057 - SPRINTER® LEGEND | 2025-09-29 BALLOON SPL15012X SPR LEG RX US M |