Primary Device ID | 00681490023900 |
NIH Device Record Key | 980a1420-3b16-4c4e-a26c-c1acefa548bb |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 05116 |
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 |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com |
Length | 12 Feet |
Length | 12 Feet |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00681490023900 [Primary] |
LPB | Cardiac ablation percutaneous catheter |
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 | 2014-09-23 |
00763000812065 - NA | 2024-03-19 WRENCH KIT 5873W TORQUE STERILE MDR |
00763000812072 - NA | 2024-03-19 TOOL 6056 PINCH ON AND FIX MDR |
20763000935584 - NA | 2024-03-19 CUSTOM PACK 12F72R 10PK R-PRIME |
20763000935607 - NA | 2024-03-19 CUSTOM PACK CB12D53R1 10PK 1/4 BRIDGE |
00763000940027 - NA | 2024-03-19 CUSTOM PACK 11X43R4 180028 |
00643169983229 - Avalus™ | 2024-03-18 VALVE 40029 AVALUS AOR MMX U30 US |
00763000757199 - NanoCross™ Elite | 2024-03-18 PTA AB14W015020090 NANOCROSS 014 V06 |
00763000757205 - NanoCross™ Elite | 2024-03-18 PTA AB14W015020150 NANOCROSS 014 V06 |