Primary Device ID | 03663703001018 |
NIH Device Record Key | 90384190-352b-4b00-960f-c6f6b19f53e1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Duocentric® |
Version Model Number | 50441STER |
Catalog Number | 83503541 |
Company DUNS | 576503098 |
Company Name | ASTON MEDICAL |
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 | 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 | +33477930004 |
info@aston-medical.com |
Outer Diameter | 5 Millimeter |
Length | 35 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03663703001018 [Primary] |
KWS | Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2024-02-19 |
Device Publish Date | 2015-09-16 |
03663703001070 | Screw |
03663703001063 | Screw |
03663703001056 | Screw |
03663703001049 | Screw |
03663703001032 | Screw |
03663703001025 | Screw |
03663703001018 | Screw |
03663703001001 | Screw |
03663703000998 | Screw |
03663703000981 | Screw |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() DUOCENTRIC 79114255 4270422 Live/Registered |
ASTON MEDICAL ANCIENNEMENT SOCIETE DE GENIE MEDICAL - S.G.M. (Société Anonyme à Directoire et conseil de surveillance) 2012-05-25 |
![]() DUOCENTRIC 73416554 1402871 Live/Registered |
TROCHOCENTRIC PATENTVERWERTUNGSGESELLSCHAFT MBH 1983-03-09 |
![]() DUOCENTRIC 72237485 0826036 Dead/Expired |
REULAND ELECTRIC COMPANY 1966-01-28 |