Primary Device ID | 57117810001054 |
NIH Device Record Key | a8e19569-5ad8-4df1-866d-4f8474864807 |
Commercial Distribution Discontinuation | 2016-06-10 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Primus By Auditdata |
Version Model Number | 2000 Primus Fitting Unit Pro |
Company DUNS | 310385849 |
Company Name | Auditdata A/S |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 57117810000989 [Package] Package: [1 Units] Discontinued: 2016-06-09 Not in Commercial Distribution |
GS1 | 57117810000996 [Package] Package: [1 Units] Discontinued: 2016-06-10 Not in Commercial Distribution |
GS1 | 57117810001009 [Package] Package: [1 Units] Discontinued: 2016-06-10 Not in Commercial Distribution |
GS1 | 57117810001023 [Package] Package: [1 Units] Discontinued: 2016-06-10 Not in Commercial Distribution |
GS1 | 57117810001054 [Primary] |
EWO | Audiometer |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-07-08 |
Device Publish Date | 2016-06-09 |
05711781001739 | 2000 Primus HIT Pro |
05711781001685 | 2000 Primus Fitting Unit + |
05711781001098 | 2000 Primus Fitting Unit Ice |
05711781001050 | 2000 Primus Fitting Unit Pro |
05711781000022 | 2000 Primus HIT Unit |
57117810001054 | 2000 Primus Fitting Unit Pro |