Primary Device ID | E0HM50220371 |
NIH Device Record Key | cbbb6f79-3312-47f1-907c-931f61cdef84 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | OCTAGON Infinity BL NC ALLIGATOR Abutment GH 3.0 mm |
Version Model Number | 5022037 |
Catalog Number | 5022037 |
Company DUNS | 318034329 |
Company Name | Hager & Meisinger Gesellschaft mit beschränkter Haftung |
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 | false |
Device Combination Product | false |
Single Use | true |
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 | true |
OTC Over-The-Counter | false |
Phone | +1(508)588-3100 |
kathystrange@acesurgical.com | |
Phone | +1(508)588-3100 |
kathystrange@acesurgical.com | |
Phone | +1(508)588-3100 |
kathystrange@acesurgical.com | |
Phone | +1(508)588-3100 |
kathystrange@acesurgical.com | |
Phone | +1(508)588-3100 |
kathystrange@acesurgical.com | |
Phone | +1(508)588-3100 |
kathystrange@acesurgical.com | |
Phone | +1(508)588-3100 |
kathystrange@acesurgical.com | |
Phone | +1(508)588-3100 |
kathystrange@acesurgical.com | |
Phone | +1(508)588-3100 |
kathystrange@acesurgical.com | |
Phone | +1(508)588-3100 |
kathystrange@acesurgical.com | |
Phone | +1(508)588-3100 |
kathystrange@acesurgical.com | |
Phone | +1(508)588-3100 |
kathystrange@acesurgical.com | |
Phone | +1(508)588-3100 |
kathystrange@acesurgical.com | |
Phone | +1(508)588-3100 |
kathystrange@acesurgical.com | |
Phone | +1(508)588-3100 |
kathystrange@acesurgical.com | |
Phone | +1(508)588-3100 |
kathystrange@acesurgical.com | |
Phone | +1(508)588-3100 |
kathystrange@acesurgical.com | |
Phone | +1(508)588-3100 |
kathystrange@acesurgical.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | E0HM50220371 [Primary] |
HIBCC | XXXX50220379 [Previous] |
NHA | Abutment, Implant, Dental, Endosseous |
Steralize Prior To Use | true |
Device Is Sterile | false |
[E0HM50220371]
Moist Heat or Steam Sterilization
[E0HM50220371]
Moist Heat or Steam Sterilization
[E0HM50220371]
Moist Heat or Steam Sterilization
[E0HM50220371]
Moist Heat or Steam Sterilization
[E0HM50220371]
Moist Heat or Steam Sterilization
[E0HM50220371]
Moist Heat or Steam Sterilization
[E0HM50220371]
Moist Heat or Steam Sterilization
[E0HM50220371]
Moist Heat or Steam Sterilization
[E0HM50220371]
Moist Heat or Steam Sterilization
[E0HM50220371]
Moist Heat or Steam Sterilization
[E0HM50220371]
Moist Heat or Steam Sterilization
[E0HM50220371]
Moist Heat or Steam Sterilization
[E0HM50220371]
Moist Heat or Steam Sterilization
[E0HM50220371]
Moist Heat or Steam Sterilization
[E0HM50220371]
Moist Heat or Steam Sterilization
[E0HM50220371]
Moist Heat or Steam Sterilization
[E0HM50220371]
Moist Heat or Steam Sterilization
[E0HM50220371]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-11-08 |
Device Publish Date | 2016-09-09 |
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