| Primary Device ID | 03664539003733 |
| NIH Device Record Key | 9f1f9ef3-2a12-4a54-a9a4-4cef048d645a |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | ANCHOR BOLT |
| Catalog Number | ACS-140SMS-10 |
| Company DUNS | 268009609 |
| Company Name | DIXI MEDICAL |
| Device Count | 10 |
| 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 |
| Phone | +33381889890 |
| info@diximedical.com | |
| Phone | +33381889890 |
| info@diximedical.com | |
| Phone | +33381889890 |
| info@diximedical.com | |
| Phone | +33381889890 |
| info@diximedical.com | |
| Phone | +33381889890 |
| info@diximedical.com | |
| Phone | +33381889890 |
| info@diximedical.com | |
| Phone | +33381889890 |
| info@diximedical.com | |
| Phone | +33381889890 |
| info@diximedical.com | |
| Phone | +33381889890 |
| info@diximedical.com | |
| Phone | +33381889890 |
| info@diximedical.com | |
| Phone | +33381889890 |
| info@diximedical.com | |
| Phone | +33381889890 |
| info@diximedical.com | |
| Phone | +33381889890 |
| info@diximedical.com | |
| Phone | +33381889890 |
| info@diximedical.com | |
| Phone | +33381889890 |
| info@diximedical.com |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 03664539003689 [Primary] |
| GS1 | 03664539003733 [Unit of Use] |
| GZL | Electrode, Depth |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-10-18 |
| Device Publish Date | 2022-10-10 |
| 03664539004037 - NA | 2024-10-01 SUBDURAL ELECTRODE WITH CONNECTION CABLE, STRIP, 1x4 CONTACTS |
| 03664539004044 - NA | 2024-10-01 SUBDURAL ELECTRODE WITH CONNECTION CABLE, STRIP, 1x6 CONTACTS |
| 03664539004051 - NA | 2024-10-01 SUBDURAL ELECTRODE WITH CONNECTION CABLE, STRIP, 1x8 CONTACTS |
| 03664539004068 - NA | 2024-10-01 SUBDURAL ELECTRODE WITH CONNECTION CABLE, GRID, 2x4 CONTACTS |
| 03664539004075 - NA | 2024-10-01 SUBDURAL ELECTRODE WITH CONNECTION CABLE, GRID, 2x6 CONTACTS |
| 03664539004082 - NA | 2024-10-01 SUBDURAL ELECTRODE WITH CONNECTION CABLE, GRID, 2x8 CONTACTS |
| 03664539004099 - NA | 2024-10-01 SUBDURAL ELECTRODE WITH CONNECTION CABLE, GRID, 4x4 CONTACTS |
| 03664539003900 - NA | 2024-04-11 GUIDE FOR Ø 2.45MM ACCESSORIES ACCESSORY OF MICRODEEP DEPTH ELECTRODE |