Primary Device ID | 07640156473421 |
NIH Device Record Key | 702cb36a-29b6-4e10-91d8-f271b2609662 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Gingivaformer |
Version Model Number | 4.03.554 |
Company DUNS | 481614829 |
Company Name | Thommen Medical AG |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07640156473421 [Primary] |
DZE | Implant, Endosseous, Root-Form |
Steralize Prior To Use | true |
Device Is Sterile | false |
[07640156473421]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-12-07 |
Device Publish Date | 2015-09-24 |
07640156478600 | 4.03.558 |
07640156478594 | 4.03.548 |
07640156478587 | 4.03.538 |
07640156473612 | 4.03.520 |
07640156473605 | 4.03.521 |
07640156473599 | 4.03.522 |
07640156473582 | 4.03.523 |
07640156473575 | 4.03.524 |
07640156473568 | 4.03.530 |
07640156473551 | 4.03.531 |
07640156473544 | 4.03.532 |
07640156473537 | 4.03.533 |
07640156473520 | 4.03.534 |
07640156473513 | 4.03.540 |
07640156473506 | 4.03.541 |
07640156473490 | 4.03.542 |
07640156473483 | 4.03.543 |
07640156473476 | 4.03.544 |
07640156473469 | 4.03.550 |
07640156473452 | 4.03.551 |
07640156473445 | 4.03.552 |
07640156473438 | 4.03.553 |
07640156473421 | 4.03.554 |
07640156473414 | 4.03.570 |
07640156473407 | 4.03.571 |
07640156473391 | 4.03.572 |
07640156473384 | 4.03.573 |
07640156473377 | 4.03.574 |
07640156471915 | 4.03.525 |
07640156471908 | 4.03.535 |