Primary Device ID | J003C0321000210001 |
NIH Device Record Key | 6d396957-710f-409e-9206-e56160b53dab |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Unimetric T Demo Kit |
Version Model Number | C032100021000 |
Catalog Number | C032100021000 |
Company DUNS | 480538495 |
Company Name | MAILLEFER INSTRUMENTS HOLDING Sàrl |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
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 |
Special Storage Condition, Specify | Between 0 and 0 *N/A |
Special Storage Condition, Specify | Between 0 and 0 *N/A |
Special Storage Condition, Specify | Between 0 and 0 *N/A |
Special Storage Condition, Specify | Between 0 and 0 *N/A |
Special Storage Condition, Specify | Between 0 and 0 *N/A |
Special Storage Condition, Specify | Between 0 and 0 *N/A |
Special Storage Condition, Specify | Between 0 and 0 *N/A |
Special Storage Condition, Specify | Between 0 and 0 *N/A |
Special Storage Condition, Specify | Between 0 and 0 *N/A |
Special Storage Condition, Specify | Between 0 and 0 *N/A |
Special Storage Condition, Specify | Between 0 and 0 *N/A |
Device Issuing Agency | Device ID |
---|---|
HIBCC | J003C0321000210001 [Primary] |
ELR | POST, ROOT CANAL |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-11-28 |
Device Publish Date | 2022-11-20 |
J003C0321000210001 | Endodontic Posts Set |
J003C0321000208001 | Endodontic Posts Set |