| Primary Device ID | 04063574200296 |
| NIH Device Record Key | 2731a08e-67a6-47bc-961f-e8cf1ef6ee73 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | nextaro® va |
| Version Model Number | 88355 |
| Company DUNS | 315549311 |
| Company Name | sfm medical devices GmbH |
| 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 | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04063574200296 [Primary] |
| LHI | Set, I.V. Fluid Transfer |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-08-25 |
| Device Publish Date | 2023-08-17 |
| 04063574100022 | nextaro® va (with 15µm filter, nominal for a 20mm vial) |
| 04063574200296 | nextaro® va (with 15µm filter, nominal for a 20mm vial) |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() NEXTARO 79345253 not registered Live/Pending |
sfm medical devices GmbH 2022-06-01 |