| Primary Device ID | 20853620005368 |
| NIH Device Record Key | 7796405f-2ae9-47fa-b391-604cab127ab1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Extension Set Regular Bore Needlefree |
| Version Model Number | 077795081000 |
| Company DUNS | 093370369 |
| Company Name | Merit Pharmaceutical |
| 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 | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Phone | (323) 227-4831 |
| solutions@meritpharm.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00853620005364 [Primary] |
| GS1 | 10853620005361 [Package] Contains: 00853620005364 Package: [50 Units] In Commercial Distribution |
| GS1 | 20853620005368 [Package] Contains: 10853620005361 Package: [4 Units] In Commercial Distribution |
| FPA | Set, Administration, Intravascular |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-02-01 |
| Device Publish Date | 2019-01-01 |
| 20853620005337 - IV Administration Set 60 Drop | 2020-05-04 |
| 10853620005439 - Needleless Neutral Valve | 2020-05-04 |
| 20853620005429 - IV Catheter Safety Winged 24G x 3/4 | 2020-05-01 |
| 20853620005207 - IV Set With In-Line Filter | 2019-12-11 |
| 20853620005214 - IV Set | 2019-12-11 |
| 20853620005276 - IV Administration Set | 2019-12-11 |
| 00853620005302 - Pressure Infuser 1000mL | 2019-12-11 |
| 20853620005313 - IV Administration Set Needlefree | 2019-12-11 |