Primary Device ID | EBRE450000019 |
NIH Device Record Key | 4af6fd55-92c7-4403-a83a-b6c1272143a6 |
Commercial Distribution Discontinuation | 2019-04-02 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Vario-Soft 3, bridge-sectionin |
Version Model Number | 45000001 |
Catalog Number | 45000001 |
Company DUNS | 341086190 |
Company Name | bredent GmbH & Co. KG |
Device Count | 1 |
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 |
Outer Diameter | 1.8 Millimeter |
Outer Diameter | 1.8 Millimeter |
Outer Diameter | 1.8 Millimeter |
Outer Diameter | 1.8 Millimeter |
Device Issuing Agency | Device ID |
---|---|
HIBCC | EBRE450000010 [Primary] |
HIBCC | EBRE450000019 [Package] Contains: EBRE450000010 Package: dummy [1 Units] Discontinued: 2016-09-22 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 | 2016-09-22 |
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