Primary Device ID | 04046964163463 |
NIH Device Record Key | caf8f6a3-8c80-45d1-bc95-18ccba5afcad |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Metha® MONO |
Version Model Number | NC310T |
Catalog Number | NC310T |
Company DUNS | 315018218 |
Company Name | Aesculap AG |
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 | 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 | +1(800)282-9000 |
GUDID.BBMUS_Service@bbraun.com | |
Phone | +1(800)282-9000 |
GUDID.BBMUS_Service@bbraun.com | |
Phone | +1(800)282-9000 |
GUDID.BBMUS_Service@bbraun.com | |
Phone | +1(800)282-9000 |
GUDID.BBMUS_Service@bbraun.com | |
Phone | +1(800)282-9000 |
GUDID.BBMUS_Service@bbraun.com | |
Phone | +1(800)282-9000 |
GUDID.BBMUS_Service@bbraun.com | |
Phone | +1(800)282-9000 |
GUDID.BBMUS_Service@bbraun.com | |
Phone | +1(800)282-9000 |
GUDID.BBMUS_Service@bbraun.com | |
Phone | +1(800)282-9000 |
GUDID.BBMUS_Service@bbraun.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04046964163463 [Primary] |
LWJ | Prosthesis, hip, semi-constrained, metal/polymer, uncemented |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2024-11-20 |
Device Publish Date | 2015-07-26 |
04046964163470 | METHA µCAP 12/14 120°/0° SIZE 1 +5MM |
04046964163463 | METHA µCAP 12/14 120°/0° SIZE 0 +5MM |
04046963914257 | METHA µCAP 12/14 120°/0° SIZE 4 |
04046963914240 | METHA µCAP 12/14 120°/0° SIZE 3 |
04046963347307 | METHA µCAP 12/14 135°/0° SIZE 5 |
04046963347246 | METHA µCAP 12/14 130°/0° SIZE 5 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
METHA 79014971 3249770 Live/Registered |
Aesculap AG 2005-07-11 |
METHA 74732503 not registered Dead/Abandoned |
ULIXES S.A. 1995-09-08 |