Primary Device ID | 20603295171499 |
NIH Device Record Key | 06a20ae9-23dc-48d1-86fe-5069097033e3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | KAMVAC |
Version Model Number | 5300-00-500 |
Catalog Number | 530000500 |
Company DUNS | 080506581 |
Company Name | DEPUY ORTHOPAEDICS, INC. |
Device Count | 1 |
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 | true |
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)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10603295171492 [Primary] |
GS1 | 20603295171499 [Package] Contains: 10603295171492 Package: BOX [20 Units] In Commercial Distribution |
JOL | CATHETER AND TIP, SUCTION |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2022-07-04 |
Device Publish Date | 2016-06-30 |
20603295171512 | KAMVAC CURVED MINI SUCTION TUBE |
20603295171505 | KAMVAC MINI SUCTION TUBE |
20603295171499 | KAMVAC STANDARD SUCTION TUBE |