Primary Device ID | 00643169615373 |
NIH Device Record Key | cdc954ec-fbf7-4291-80cb-dc546f99e4c1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ThoraTrak™ |
Version Model Number | 28604 |
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 | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00643169615373 [Direct Marking] |
GS1 | 00763000058319 [Primary] |
GAD | RETRACTOR |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00643169615373]
Moist Heat or Steam Sterilization
[00643169615373]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-02-06 |
Device Publish Date | 2018-02-16 |
00643169615410 | BLADE 28606B THORATRAK SHRT EXT INFR STD |
00643169615403 | BLADE 28604B THORATRAK LNG EXT INFR STD |
00643169615397 | BLADE 28606 THORATRAK SHRT THRCTMY DP |
00643169615380 | BLADE 28605 THORATRAK SHRT THRCTMY STD |
00643169615373 | BLADE 28604 THORATRAK LNG THRCTMY DP |
00643169615366 | BLADE 28603 THORATRAK LNG THRCTMY STD |
00643169615359 | BLADE 28602 THORATRAK LIMA DP |
00643169615342 | BLADE 28601 THORATRAK LIMA STD |
00643169615335 | RETRACTOR RACK 28611 THORATRAK |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
THORATRAK 77436684 3565785 Live/Registered |
Medtronic, Inc. 2008-04-01 |