Primary Device ID | 03664539000671 |
NIH Device Record Key | 38b99aef-c522-4dbb-9e9a-d3d1a5a4a57c |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | ANCHOR BOLT |
Catalog Number | ACS-025SMS-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 | false |
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 | |
Phone | +33381889890 |
info@diximedical.com | |
Phone | +33381889890 |
info@diximedical.com |
Length | 25 Millimeter |
Length | 25 Millimeter |
Length | 25 Millimeter |
Length | 25 Millimeter |
Length | 25 Millimeter |
Length | 25 Millimeter |
Length | 25 Millimeter |
Length | 25 Millimeter |
Length | 25 Millimeter |
Length | 25 Millimeter |
Length | 25 Millimeter |
Length | 25 Millimeter |
Length | 25 Millimeter |
Length | 25 Millimeter |
Length | 25 Millimeter |
Length | 25 Millimeter |
Length | 25 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03664539000671 [Primary] |
GS1 | 03664539003290 [Unit of Use] |
GZL | Electrode, Depth |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-09-23 |
Device Publish Date | 2017-12-14 |
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 |