Primary Device ID | 00681490881555 |
NIH Device Record Key | f1546416-94c8-4d40-b000-f9816a5f6dbb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | INVISx® |
Version Model Number | 60720 |
Company DUNS | 089055867 |
Company Name | MEDTRONIC PS MEDICAL, 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 | 00681490881555 [Primary] |
GXN | PLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00681490881555]
Moist Heat or Steam Sterilization
[00681490881555]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-08-28 |
00643169103467 | INSTR 60710 INVISX TENSIONING REUSE |
00643169498242 | SET 60700 INVISX CRNL FXTION INSTR |
00643169498006 | INSTR 60710 INVISX TENSIONING REUSE |
00643169497771 | TRAY 60730 INVISX INSTRUMENT |
20643169466306 | LOCKS 60100 INVISX 2PK CE |
00681490881579 | TRAY 60730 INVISX INSTRUMENT |
00681490881555 | INSTRUMENT 60720 INVISX TRIMMING REU |
00681490881470 | SET 60700 INVISX CRNL FXTION INSTR |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
INVISX 78043473 2660838 Live/Registered |
Medtronic, Inc. 2001-01-17 |