Primary Device ID | EBRE430073169 |
NIH Device Record Key | 1cefe66e-18e5-4888-be9f-d5ffa4f5dfd1 |
Commercial Distribution Discontinuation | 2019-04-02 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Vario-Soft 3 mini |
Version Model Number | 43007316 |
Catalog Number | 43007316 |
Company DUNS | 341086190 |
Company Name | bredent GmbH & Co. KG |
Device Count | 50 |
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 | 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 | +4907309872451 |
info@bredent.com |
Width | 3 Millimeter |
Width | 3 Millimeter |
Width | 3 Millimeter |
Device Issuing Agency | Device ID |
---|---|
HIBCC | EBRE430073160 [Primary] |
HIBCC | EBRE430073168 [Unit of Use] |
HIBCC | EBRE430073169 [Package] Contains: EBRE430073160 Package: dummy [1 Units] Discontinued: 2016-09-21 Not in Commercial Distribution |
EGG | ATTACHMENT, PRECISION, ALL |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-04-03 |
Device Publish Date | 2016-09-21 |
EBRE430073189 | Vario-Soft 3 mini Matrix, green 50 Pieces |
EBRE430073169 | Vario-Soft 3 mini Matrix, yellow 50 Pieces |
EBRE430073149 | Vario-Soft 3 mini Matrix, red 50 Pieces |
EBRE430073179 | Vario-Soft 3 mini Matrix, green 8 Pieces |
EBRE430073159 | Vario-Soft 3 mini Matrix, yellow 8 Pieces |
EBRE430073139 | Vario-Soft 3 mini Matrix, red 8 Pieces |
EBRE430073129 | Vario-Soft 3 mini 13 Parts 1 Assortment |