Primary Device ID | EHKM10071051 |
NIH Device Record Key | d176cf2a-6a10-4a8e-bb58-555d39a78b5a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NiTiBOND Nitinol/Titanium |
Version Model Number | 1007105 |
Catalog Number | 1007105 |
Company DUNS | 341155720 |
Company Name | Heinz Kurz GmbH |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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 | +49707291790 |
info@kurzmed.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | EHKM10071051 [Primary] |
ETB | Prosthesis, Partial Ossicular Replacement |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-09-21 |
EHKM10071611 | Ossicular Prosthesis, partial |
EHKM10071591 | Ossicular Prosthesis, partial |
EHKM10071581 | Ossicular Prosthesis, partial |
EHKM10071571 | Ossicular Prosthesis, partial |
EHKM10071561 | Ossicular Prosthesis, partial |
EHKM10071551 | Ossicular Prosthesis, partial |
EHKM10071541 | Ossicular Prosthesis, partial |
EHKM10071531 | Ossicular Prosthesis, partial |
EHKM10071111 | Ossicular Prosthesis, partial |
EHKM10071091 | Ossicular Prosthesis, partial |
EHKM10071081 | Ossicular Prosthesis, partial |
EHKM10071071 | Ossicular Prosthesis, partial |
EHKM10071061 | Ossicular Prosthesis, partial |
EHKM10071051 | Ossicular Prosthesis, partial |
EHKM10071041 | Ossicular Prosthesis, partial |
EHKM10071031 | Ossicular Prosthesis, partial |