Removal adapter, CONELOG® C5302.5001

GUDID E219C530250011

Removal adapter, CONELOG®, d 5.0 mm

ALTATEC GmbH

Dental implant extractor
Primary Device IDE219C530250011
NIH Device Record Key7eaaf08b-0b21-4174-8d9c-89a360ba02eb
Commercial Distribution Discontinuation2025-04-03
Commercial Distribution StatusNot in Commercial Distribution
Brand NameRemoval adapter, CONELOG®
Version Model NumberC5302.5001
Catalog NumberC5302.5001
Company DUNS322018193
Company NameALTATEC GmbH
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone7609181857
Emailinfo@camlog.com
Phone7609181857
Emailinfo@camlog.com
Phone7609181857
Emailinfo@camlog.com
Phone7609181857
Emailinfo@camlog.com
Phone7609181857
Emailinfo@camlog.com
Phone7609181857
Emailinfo@camlog.com
Phone7609181857
Emailinfo@camlog.com
Phone7609181857
Emailinfo@camlog.com
Phone7609181857
Emailinfo@camlog.com
Phone7609181857
Emailinfo@camlog.com
Phone7609181857
Emailinfo@camlog.com
Phone7609181857
Emailinfo@camlog.com
Phone7609181857
Emailinfo@camlog.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCE219C530250011 [Primary]

FDA Product Code

NDPAccessories, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2025-04-04
Device Publish Date2022-12-08

On-Brand Devices [Removal adapter, CONELOG®]

E219C530250011Removal adapter, CONELOG®, d 5.0 mm
E219C530243011Removal adapter, CONELOG®, d 3.8/4.3mm
E219C530233011Removal adapter, CONELOG®, d 3.3

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.