Primary Device ID | 20643169423170 |
NIH Device Record Key | 41a7e3ee-a47a-4d50-a67a-9d227d389867 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CLEARVIEW® |
Version Model Number | 22120 |
Company DUNS | 006261481 |
Company Name | MEDTRONIC, INC. |
Device Count | 10 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |
OTC Over-The-Counter | false |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00643169423176 [Unit of Use] |
GS1 | 20643169423170 [Primary] |
FQH | LAVAGE, JET |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2017-01-03 |
20885074257475 | SHUNT, ARTERIOTOMY 31300 -3.00MM, 15LA |
20643169423170 | BLOWER/MISTER KIT 22120 CLEARVIEW 10P 15 |
00885074257464 | SHUNT 31275 ARTERIOTOMY 2.75MM 5PK 15LA |
00885074257457 | SHUNT 31250 ARTERIOTOMY 2.50MM 5PK 15LA |
00885074257440 | SHUNT 31225 ARTERIOTOMY 2.25MM 5PK 15LA |
00885074257433 | SHUNT 31200 ARTERIOTOMY 2.00MM 5PK 15LA |
00885074257426 | SHUNT 31175 ARTERIOTOMY 1.75MM 5PK 15LA |
00885074257419 | SHUNT 31150 ARTERIOTOMY 1.50MM 5PK 15LA |
00885074257402 | SHUNT 31125 ARTERIOTOMY 1.25MM 5PK 15LA |
00885074257112 | SHUNT 31100 ARTERIOTOMY 1.00MM 5 PK 15LA |