Primary Device ID | 06009544040934 |
NIH Device Record Key | 958ba6a9-15c1-431b-b693-2b01b18fcbc5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PROVATA® |
Version Model Number | MSC-PRO618 |
Company DUNS | 636239584 |
Company Name | SOUTHERN IMPLANTS (PTY) LTD |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06009544040934 [Primary] |
DZE | Implant, Endosseous, Root-Form |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-07-29 |
Device Publish Date | 2022-07-21 |
06009544040934 | PROVATA® MSc Implant, Ø6.0 x 18mm |
06009544040927 | PROVATA® MSc Implant, Ø6.0 x 15mm |
06009544040910 | PROVATA® MSc Implant, Ø6.0 x 13mm |
06009544040903 | PROVATA® MSc Implant, Ø6.0 x 11mm |
06009544040880 | PROVATA® MSc Implant, Ø6.0 x 8mm |
06009544040897 | PROVATA® MSc Implant, Ø6.0 x 10mm |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PROVATA 87941994 5754979 Live/Registered |
The Staywell Company, LLC 2018-05-30 |
PROVATA 87822119 5758845 Live/Registered |
Southern Implants (Pty) Ltd. 2018-03-06 |
PROVATA 86270018 5008520 Live/Registered |
Oliveri, Joe 2014-05-02 |
PROVATA 76561176 not registered Dead/Abandoned |
Nissan Chemical Industries, Ltd. 2003-11-21 |
PROVATA 75897947 not registered Dead/Abandoned |
Nissan Chemical Industries, Ltd. 2000-01-18 |