Primary Device ID | E219J370900151 |
NIH Device Record Key | 6dfd86f6-59fd-464e-9ff4-5e4be42f200d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Universal holder |
Version Model Number | J3709.0015 |
Catalog Number | J3709.0015 |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 9999999999 |
info@camlog.com | |
Phone | 9999999999 |
info@camlog.com | |
Phone | 9999999999 |
info@camlog.com | |
Phone | 9999999999 |
info@camlog.com | |
Phone | 9999999999 |
info@camlog.com | |
Phone | 9999999999 |
info@camlog.com | |
Phone | 9999999999 |
info@camlog.com | |
Phone | 9999999999 |
info@camlog.com | |
Phone | 9999999999 |
info@camlog.com | |
Phone | 9999999999 |
info@camlog.com | |
Phone | 9999999999 |
info@camlog.com | |
Phone | 9999999999 |
info@camlog.com | |
Phone | 9999999999 |
info@camlog.com | |
Phone | 9999999999 |
info@camlog.com | |
Phone | 9999999999 |
info@camlog.com | |
Phone | 9999999999 |
info@camlog.com | |
Phone | 9999999999 |
info@camlog.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | E219J370900151 [Primary] |
NDP | Accessories, Implant, Dental, Endosseous |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-09-14 |
Device Publish Date | 2023-09-06 |
E219J370900151 | Universal holder |
E219J370900101 | Universal holder incl. abutment collects Ø 3.3/3.8/4.3/5.0/6.0 mm |