Primary Device ID | E165600137010 |
NIH Device Record Key | afec6f25-104a-4191-8ddd-40215ad26340 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ROEKO GuttaFlow®2 |
Version Model Number | STANDARD SET |
Catalog Number | 60013701 |
Company DUNS | 315494443 |
Company Name | Coltène/Whaledent 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 | true |
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 | +4973458050 |
info.de@coltene.com |
Special Storage Condition, Specify | Between 0 and 0 *keep away from sunlight |
Device Issuing Agency | Device ID |
---|---|
HIBCC | E165600137010 [Primary] |
EKM | Gutta-Percha |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-12-29 |
E165600195290 | SAMPLE |
E165600137450 | REFILL PACK DUAL-BARREL SYRING |
E165600137060 | REFILL PACK CAPSULES FAST |
E165600137040 | REFILL PACK CAPSULES REGULAR |
E165600137020 | The ROEKO GuttaFlow®2 Introkit contains 1 x Capsules GuttaFlow®2 (20 pcs), 1 x Canal Tips + St |
E165600137010 | STANDARD SET |
E165600137190 | ROEKO GuttaFlow®2 Mixing tips |