Primary Device ID | E226035212A11 |
NIH Device Record Key | ebf1612d-fc8b-4690-a894-6e511bbb316f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | KOMET CeraDrill |
Version Model Number | K210L20.205.042.A1 |
Catalog Number | K210L20.205.042 |
Company DUNS | 317409001 |
Company Name | Gebr. Brasseler GmbH & Co. KG |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 | E226035212A11 [Primary] |
EJL | BUR, DENTAL |
Steralize Prior To Use | true |
Device Is Sterile | false |
[E226035212A11]
Moist Heat or Steam Sterilization
[E226035212A11]
Moist Heat or Steam Sterilization
[E226035212A11]
Moist Heat or Steam Sterilization
[E226035212A11]
Moist Heat or Steam Sterilization
[E226035212A11]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-02-09 |
Device Publish Date | 2023-02-01 |
E226035212A11 | K210L20.205.042.A1 |
E226035211A11 | K210L20.205.035.A1 |
E226034900A11 | K210L20.205.028.A1 |
E226034899A11 | K210L20.205.020.A1 |
E226033794A11 | K210L16.204.028.A1 |
E226033793A11 | K210L19.204.020.A1 |
E226033792A11 | K210L16.204.020.A1 |
E226033795A11 | K210L19.204.028.A1 |