Primary Device ID | 10886705029921 |
NIH Device Record Key | 31b97231-7183-40c3-a491-dd9d3dbf2166 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HEALIX TI 3 SUTURE ANCHOR w/DYNACORD |
Version Model Number | 222052 |
Catalog Number | 222052 |
Company DUNS | 482661753 |
Company Name | Medos International Sàrl |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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 | |
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 | 10886705029921 [Primary] |
HWC | Screw, fixation, bone |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-10-02 |
Device Publish Date | 2020-09-24 |
10886705029983 | HEALIX TI 3 SUTURE ANCHOR w/DYNACORD Titanium Anchor (1) Blue (1) White/Blue/Green Striped (1) W |
10886705029952 | HEALIX TI 3 SUTURE ANCHOR w/DYNACORD Titanium Anchor (1) Blue (1) White/Blue/Green Striped (1) W |
10886705029921 | HEALIX TI 3 SUTURE ANCHOR w/DYNACORD Titanium Anchor (1) Blue (1) White/Blue/Green Striped (1) W |