Primary Device ID | E29967369 |
NIH Device Record Key | 1cbd74bf-b9ac-4101-baa9-769aad297689 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Lumicontrast sectional matrices |
Version Model Number | 6736 |
Company DUNS | 481461598 |
Company Name | Polydentia SA |
Device Count | 70 |
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 | 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 |
Phone | +41919462948 |
info@polydentia.ch | |
Phone | +41919462948 |
info@polydentia.ch | |
Phone | +41919462948 |
info@polydentia.ch | |
Phone | +41919462948 |
info@polydentia.ch | |
Phone | +41919462948 |
info@polydentia.ch | |
Phone | +41919462948 |
info@polydentia.ch | |
Phone | +41919462948 |
info@polydentia.ch | |
Phone | +41919462948 |
info@polydentia.ch |
Device Issuing Agency | Device ID |
---|---|
HIBCC | E29967360 [Primary] |
HIBCC | E29967369 [Unit of Use] |
DZN | Instruments, Dental Hand |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-07-14 |
Device Publish Date | 2022-07-06 |
E29967469 | 0.04 mm / 6.4 mm + Ext., 25 pcs. |
E29967569 | 0.025 mm / 6.4mm +ext, 50 pcs. |
E29967369 | 0.025 mm / 6.4 mm, 70 pcs. |
E29967359 | 0.025 mm / 5 mm, 70 pcs. |
E29967069 | 0.04 mm / 6.4 mm, 35 pcs. |
E29967059 | 0.04 mm / 5 mm, 35 pcs. |