Primary Device ID | E22120491 |
NIH Device Record Key | f2f89c54-67ec-4707-9f88-dfa18a1c22bc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Trimming disc |
Version Model Number | 2049 |
Catalog Number | 2049 |
Company DUNS | 316699578 |
Company Name | VOCO GmbH |
Device Count | 10 |
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 | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 999-999-9999 |
xxx@xx.xx |
Storage Environment Temperature | Between 4 Degrees Celsius and 23 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
HIBCC | E2212049 [Unit of Use] |
HIBCC | E22120491 [Primary] |
EHL | Point, Abrasive |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-03-23 |
Device Publish Date | 2019-06-06 |
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