Primary Device ID | 00643169504929 |
NIH Device Record Key | 92b527f5-bbb0-4295-a66c-47cfb64d39c8 |
Commercial Distribution Discontinuation | 2019-03-15 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Freezor® MAX |
Version Model Number | 229F3 |
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 | 90 Centimeter |
Length | 90 Centimeter |
Length | 90 Centimeter |
Length | 90 Centimeter |
Length | 90 Centimeter |
Length | 90 Centimeter |
Length | 90 Centimeter |
Length | 90 Centimeter |
Handling Environment Humidity | Between 0 Percent (%) Relative Humidity and 85 Percent (%) Relative Humidity |
Handling Environment Humidity | Between 0 Percent (%) Relative Humidity and 85 Percent (%) Relative Humidity |
Handling Environment Humidity | Between 0 Percent (%) Relative Humidity and 85 Percent (%) Relative Humidity |
Handling Environment Humidity | Between 0 Percent (%) Relative Humidity and 85 Percent (%) Relative Humidity |
Handling Environment Humidity | Between 0 Percent (%) Relative Humidity and 85 Percent (%) Relative Humidity |
Handling Environment Humidity | Between 0 Percent (%) Relative Humidity and 85 Percent (%) Relative Humidity |
Handling Environment Humidity | Between 0 Percent (%) Relative Humidity and 85 Percent (%) Relative Humidity |
Handling Environment Humidity | Between 0 Percent (%) Relative Humidity and 85 Percent (%) Relative Humidity |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00643169504929 [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 | 4 |
Public Version Date | 2019-06-12 |
Device Publish Date | 2015-09-18 |
00613994804273 | CATHETER 239F3 FREEZOR MAX3 MED BLUE 9F |
00643169023505 | CATH 229F3 FREEZOR MAX3 SURGICAL MED 9F |
00643169023499 | CATH 229F5 FREEZOR MAX5 SURGICAL LG 9F |
00643169023482 | CATHETER 239F3 FREEZOR MAX3 MED BLUE 9F |
00643169023475 | CATHETER 239F5 FREEZOR MAX5 LG ORANGE9F |
00643169504929 | CATH 229F3 FREEZOR MAX3 SURGICAL MED 9F |
00643169504912 | CATH 229F5 FREEZOR MAX5 SURGICAL LG 9F |
00643169504905 | CATHETER 239F3 FREEZOR MAX3 MED BLUE 9F |
00643169504899 | CATHETER 239F5 FREEZOR MAX5 LG ORANGE9F |
00643169450387 | CATHETER 239F5 FREEZOR MAX5 LG ORANGE9F |
00643169450370 | CATHETER 239F3 FREEZOR MAX3 MED BLUE 9F |
00643169450363 | CATH 229F5 FREEZOR MAX5 SURGICAL LG 9F |
00643169450356 | CATH 229F3 FREEZOR MAX3 SURGICAL MED 9F |
00763000245474 | CATHETER 239F3 FREEZOR MAX3 MED BLUE 9F |
00763000245481 | CATHETER 239F5 FREEZOR MAX5 LG ORANGE9F |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() FREEZOR 75664372 2498756 Live/Registered |
MEDTRONIC CRYOCATH LP 1999-03-19 |