Primary Device ID | E219C530250011 |
NIH Device Record Key | 7eaaf08b-0b21-4174-8d9c-89a360ba02eb |
Commercial Distribution Discontinuation | 2025-04-03 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Removal adapter, CONELOG® |
Version Model Number | C5302.5001 |
Catalog Number | C5302.5001 |
Company DUNS | 322018193 |
Company Name | ALTATEC GmbH |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 | 7609181857 |
info@camlog.com | |
Phone | 7609181857 |
info@camlog.com | |
Phone | 7609181857 |
info@camlog.com | |
Phone | 7609181857 |
info@camlog.com | |
Phone | 7609181857 |
info@camlog.com | |
Phone | 7609181857 |
info@camlog.com | |
Phone | 7609181857 |
info@camlog.com | |
Phone | 7609181857 |
info@camlog.com | |
Phone | 7609181857 |
info@camlog.com | |
Phone | 7609181857 |
info@camlog.com | |
Phone | 7609181857 |
info@camlog.com | |
Phone | 7609181857 |
info@camlog.com | |
Phone | 7609181857 |
info@camlog.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | E219C530250011 [Primary] |
NDP | Accessories, Implant, Dental, Endosseous |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2025-04-04 |
Device Publish Date | 2022-12-08 |
E219C530250011 | Removal adapter, CONELOG®, d 5.0 mm |
E219C530243011 | Removal adapter, CONELOG®, d 3.8/4.3mm |
E219C530233011 | Removal adapter, CONELOG®, d 3.3 |