Primary Device ID | EHKM10072571 |
NIH Device Record Key | 6c6511db-f519-46a9-b02a-8917a512f373 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NiTiFLEX Nitinol/Titanium |
Version Model Number | 1007257 |
Catalog Number | 1007257 |
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 | EHKM10072571 [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 |
EHKM10072611 | Ossicular Prosthesis, partial |
EHKM10072591 | Ossicular Prosthesis, partial |
EHKM10072581 | Ossicular Prosthesis, partial |
EHKM10072571 | Ossicular Prosthesis, partial |
EHKM10072561 | Ossicular Prosthesis, partial |
EHKM10072551 | Ossicular Prosthesis, partial |
EHKM10072541 | Ossicular Prosthesis, partial |
EHKM10072531 | Ossicular Prosthesis, partial |
EHKM10072111 | Ossicular Prosthesis, partial |
EHKM10072091 | Ossicular Prosthesis, partial |
EHKM10072081 | Ossicular Prosthesis, partial |
EHKM10072071 | Ossicular Prosthesis, partial |
EHKM10072061 | Ossicular Prosthesis, partial |
EHKM10072051 | Ossicular Prosthesis, partial |
EHKM10072041 | Ossicular Prosthesis, partial |
EHKM10072031 | Ossicular Prosthesis, partial |