Primary Device ID | E29961079 |
NIH Device Record Key | f52bf2d4-632a-4662-8a6b-9c5a57be22b1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | contoured tofflemire matrices |
Version Model Number | 6107 |
Company DUNS | 481461598 |
Company Name | Polydentia SA |
Device Count | 30 |
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 | E29961070 [Primary] |
HIBCC | E29961079 [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 |
E29961099 | 0.025 mm / 5.5 mm, 30 pcs. |
E29961089 | 0.025 mm / 6.3 mm, 30 pcs. |
E29961079 | 0.04 mm / 5.5 mm, 30 pcs. |
E29961069 | 0.04 mm / 6.3 mm, 30 pcs. |