Primary Device ID | J014660802910 |
NIH Device Record Key | 76a0f6b7-d844-4ea6-a502-457e0d787191 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Artic digital 6, A2 / TO05D, CE |
Version Model Number | 66080291 |
Catalog Number | 66080291 |
Company DUNS | 315666321 |
Company Name | Heraeus Kulzer GmbH |
Device Count | 1 |
DM Exempt | true |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | J014660802910 [Primary] |
ELM | Denture, plastic, teeth |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-09-03 |
Device Publish Date | 2024-08-26 |
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