| Primary Device ID | 20886705030023 |
| NIH Device Record Key | af54e776-7771-4db5-99e9-f505920c92a4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DYNACORD |
| Version Model Number | 222068 |
| Catalog Number | 222068 |
| Company DUNS | 482661753 |
| Company Name | Medos International Sàrl |
| Device Count | 12 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| 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 | |
| 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 | 10886705030026 [Unit of Use] |
| GS1 | 20886705030023 [Primary] |
| GAT | SUTURE, NONABSORBABLE, SYNTHETIC, POLYETHYLENE |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-02-07 |
| Device Publish Date | 2018-11-19 |
| 20886705030054 | DYNACORD Suture 1 Blue and 1 White/Blue/Green Striped Braided Composite Suture OS-6 36mm 1/2c Re |
| 20886705030047 | DYNACORD Suture 1 Blue and 1 White/Blue/Green Striped Braided Composite Suture MO-7 22mm 1/2c Ta |
| 20886705030030 | DYNACORD Suture 1 Blue and 1 White/Blue/Green Striped Braided Composite Suture Number 2 (5 metri |
| 20886705030023 | DYNACORD Suture White/Blue/Green Striped Braided Composite Suture Number 2 (5 metric), 36 inches |
| 20886705030016 | DYNACORD Suture Blue Braided Composite Suture Number 2 (5 metric), 36 inches (91 cm) |
| 20886705030009 | DYNACORD Suture Blue Braided Composite Suture MO-7 22mm 1/2c Taper N=1 Number 2 (5 metric), 36 i |
| 20886705029997 | DYNACORD Suture Blue Braided Composite Suture OS-6 36mm 1/2c Reverse Cutting N=1 Number 2 (5 met |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() DYNACORD 87361033 5581562 Live/Registered |
Johnson & Johnson 2017-03-07 |
![]() DYNACORD 87235522 not registered Dead/Abandoned |
EVI Audio Gmbh 2016-11-14 |
![]() DYNACORD 86088790 not registered Dead/Abandoned |
DePuy Synthes, Inc. 2013-10-10 |
![]() DYNACORD 79216225 5537734 Live/Registered |
EVI Audio GmbH 2017-07-28 |
![]() DYNACORD 74591966 1950695 Dead/Cancelled |
BOSCH SECURITY SYSTEMS, INC. 1994-10-28 |
![]() DYNACORD 73699354 1500329 Dead/Cancelled |
DYNACORD ELECTRONIC- UND GERATEBAU GMBH& CO. KG 1987-12-07 |
![]() DYNACORD 72171714 0780568 Live/Registered |
Sternberg, Bela 1963-06-24 |
![]() DYNACORD 72171713 0780621 Dead/Expired |
BELA STERNBERG, DOING BUSINESS AS HALIFAX DISTRIBUTING COMPANY 1963-06-24 |
![]() DYNACORD 72143581 0755006 Dead/Expired |
TORPEDO BUROMASCHINEN WERKE A.G. 1962-05-01 |