| Primary Device ID | 26955739013501 |
| NIH Device Record Key | e04ef6a2-5578-41bb-988e-7436540352b0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Natus |
| Version Model Number | 017505 |
| Company DUNS | 529249095 |
| Company Name | Xi'an Friendship Medical Electronics Co.,Ltd. |
| 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 | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 16955739013504 [Primary] |
| GS1 | 26955739013501 [Package] Contains: 16955739013504 Package: Box [24 Units] In Commercial Distribution |
| GXZ | Electrode, Needle |
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[26955739013501]
Ethylene Oxide
[26955739013501]
Ethylene Oxide
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2017-12-28 |