| Primary Device ID | 10842289102603 |
| NIH Device Record Key | c39537c2-7e99-44ce-822e-066b9549d43d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Medic Anti-stick Needle/Connector |
| Version Model Number | M8-5007 |
| Company DUNS | 088013219 |
| Company Name | NXSTAGE MEDICAL, INC. |
| Device Count | 250 |
| 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 | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | 1-866-697-8243 |
| info@nxstage.com |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00842289102606 [Primary] |
| GS1 | 00842289103030 [Unit of Use] |
| GS1 | 10842289102603 [Package] Contains: 00842289102606 Package: Shipping Box [4 Units] In Commercial Distribution |
| FMI | Needle, Hypodermic, Single Lumen |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-10-20 |
| Device Publish Date | 2020-10-12 |
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| 00842289104044 - VersiHD with GuideMe Software | 2025-10-01 |
| 00842289104051 - VersiHD with GuideMe Software | 2025-10-01 |
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| 00842289103887 - NXSTAGE CARTRIDGE EXPRESS | 2024-08-01 |
| 10842289103044 - NxStage PureFlow Solution | 2024-04-04 |
| 10842289103051 - NxStage PureFlow Solution | 2024-04-04 |