Primary Device ID | 06009544016441 |
NIH Device Record Key | 31c4519c-a2d0-4512-ae18-d1dffc455a4e |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | MC-DC4-5 |
Company DUNS | 636239584 |
Company Name | SOUTHERN IMPLANTS (PTY) 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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06009544016441 [Primary] |
NHA | Abutment, Implant, Dental, Endosseous |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-11-08 |
Device Publish Date | 2019-01-08 |
06009544038252 - NA | 2024-11-06 Screw Ti Hex Series L3.5mm |
06009544039952 - N/A | 2024-11-01 Screw Titanium Hex 1 Series ø2.7 Head |
06009544039969 - N/A | 2024-11-01 Screw Ti Hexed M1.4 NLT |
06009544048589 - N/A | 2024-09-03 Implant SP1 Ø4.0x10mm |
06009544048596 - N/A | 2024-09-03 Implant SP1 Ø4.0x11mm |
06009544048619 - N/A | 2024-09-03 Implant SP1 Ø4.0x15mm |
06009544048626 - N/A | 2024-09-03 Implant SP1 Ø4.0x18mm |
06009544048633 - N/A | 2024-09-03 Implant SP1 Ø4.0x20mm |