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 |
00842289103870 - NXSTAGE CARTRIDGE EXPRESS | 2024-08-01 |
00842289103887 - NXSTAGE CARTRIDGE EXPRESS | 2024-08-01 |
10842289103044 - NxStage PureFlow Solution | 2024-04-04 |
10842289103051 - NxStage PureFlow Solution | 2024-04-04 |
10842289103068 - NxStage PureFlow Solution | 2024-04-04 |
10842289103075 - NxStage PureFlow Solution | 2024-04-04 |
10842289103082 - NxStage PureFlow Solution | 2024-04-04 |
10842289103099 - NxStage PureFlow Solution | 2024-04-04 |