Primary Device ID | EBGOFLPCC201 |
NIH Device Record Key | 9a0a4722-79aa-4ff9-914b-88bfc4c91bf7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Permanent Crown C2 |
Version Model Number | FLPCC201US |
Company DUNS | 316483072 |
Company Name | BEGO Bremer Goldschlägerei Wilh. Herbst GmbH & Co.KG |
Device Count | 1 |
DM Exempt | false |
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 | 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 | +4942120280 |
info@bego.com | |
Phone | +4942120280 |
info@bego.com | |
Phone | +4942120280 |
info@bego.com | |
Phone | +4942120280 |
info@bego.com | |
Phone | +4942120280 |
info@bego.com | |
Phone | +4942120280 |
info@bego.com | |
Phone | +4942120280 |
info@bego.com | |
Phone | +4942120280 |
info@bego.com | |
Phone | +4942120280 |
info@bego.com | |
Phone | +4942120280 |
info@bego.com | |
Phone | +4942120280 |
info@bego.com | |
Phone | +4942120280 |
info@bego.com | |
Phone | +4942120280 |
info@bego.com | |
Phone | +4942120280 |
info@bego.com | |
Phone | +4942120280 |
info@bego.com | |
Phone | +4942120280 |
info@bego.com | |
Phone | +4942120280 |
info@bego.com | |
Phone | +4942120280 |
info@bego.com | |
Phone | +4942120280 |
info@bego.com | |
Phone | +4942120280 |
info@bego.com |
Special Storage Condition, Specify | Between 0 and 0 *Dry |
Special Storage Condition, Specify | Between 0 and 0 *Dry |
Special Storage Condition, Specify | Between 0 and 0 *Dry |
Special Storage Condition, Specify | Between 0 and 0 *Dry |
Special Storage Condition, Specify | Between 0 and 0 *Dry |
Special Storage Condition, Specify | Between 0 and 0 *Dry |
Special Storage Condition, Specify | Between 0 and 0 *Dry |
Special Storage Condition, Specify | Between 0 and 0 *Dry |
Special Storage Condition, Specify | Between 0 and 0 *Dry |
Special Storage Condition, Specify | Between 0 and 0 *Dry |
Special Storage Condition, Specify | Between 0 and 0 *Dry |
Special Storage Condition, Specify | Between 0 and 0 *Dry |
Special Storage Condition, Specify | Between 0 and 0 *Dry |
Special Storage Condition, Specify | Between 0 and 0 *Dry |
Special Storage Condition, Specify | Between 0 and 0 *Dry |
Special Storage Condition, Specify | Between 0 and 0 *Dry |
Special Storage Condition, Specify | Between 0 and 0 *Dry |
Special Storage Condition, Specify | Between 0 and 0 *Dry |
Special Storage Condition, Specify | Between 0 and 0 *Dry |
Special Storage Condition, Specify | Between 0 and 0 *Dry |
Device Issuing Agency | Device ID |
---|---|
HIBCC | EBGOFLPCC201 [Primary] |
EBF | Material, Tooth Shade, Resin |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-10-27 |
Device Publish Date | 2020-10-19 |
EBGOFLPCC201 | FLPCC201US |
EBGOFLPCC201US1 | FLPCC201US |