| Primary Device ID | ENTTTHO10MI4500051 |
| NIH Device Record Key | a90edef2-33a0-48ca-b7ef-966f0d731007 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | nt-Preform® |
| Version Model Number | THO 10.MI4.500.05 |
| Catalog Number | THO 10.MI4.500.05 |
| Company DUNS | 312800478 |
| Company Name | NT-Trading GmbH & Co. KG |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| 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 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 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 Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | ENTTTHO10MI4500051 [Primary] |
| NHA | ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[ENTTTHO10MI4500051]
Dry Heat Sterilization
[ENTTTHO10MI4500051]
Dry Heat Sterilization
[ENTTTHO10MI4500051]
Dry Heat Sterilization
[ENTTTHO10MI4500051]
Dry Heat Sterilization
[ENTTTHO10MI4500051]
Dry Heat Sterilization
[ENTTTHO10MI4500051]
Dry Heat Sterilization
[ENTTTHO10MI4500051]
Dry Heat Sterilization
[ENTTTHO10MI4500051]
Dry Heat Sterilization
[ENTTTHO10MI4500051]
Dry Heat Sterilization
[ENTTTHO10MI4500051]
Dry Heat Sterilization
[ENTTTHO10MI4500051]
Dry Heat Sterilization
[ENTTTHO10MI4500051]
Dry Heat Sterilization
[ENTTTHO10MI4500051]
Dry Heat Sterilization
[ENTTTHO10MI4500051]
Dry Heat Sterilization
[ENTTTHO10MI4500051]
Dry Heat Sterilization
[ENTTTHO10MI4500051]
Dry Heat Sterilization
[ENTTTHO10MI4500051]
Dry Heat Sterilization
[ENTTTHO10MI4500051]
Dry Heat Sterilization
[ENTTTHO10MI4500051]
Dry Heat Sterilization
[ENTTTHO10MI4500051]
Dry Heat Sterilization
[ENTTTHO10MI4500051]
Dry Heat Sterilization
[ENTTTHO10MI4500051]
Dry Heat Sterilization
[ENTTTHO10MI4500051]
Dry Heat Sterilization
[ENTTTHO10MI4500051]
Dry Heat Sterilization
[ENTTTHO10MI4500051]
Dry Heat Sterilization
[ENTTTHO10MI4500051]
Dry Heat Sterilization
[ENTTTHO10MI4500051]
Dry Heat Sterilization
[ENTTTHO10MI4500051]
Dry Heat Sterilization
[ENTTTHO10MI4500051]
Dry Heat Sterilization
[ENTTTHO10MI4500051]
Dry Heat Sterilization
[ENTTTHO10MI4500051]
Dry Heat Sterilization
[ENTTTHO10MI4500051]
Dry Heat Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-11-08 |
| Device Publish Date | 2019-08-23 |