Primary Device ID | 08050705890019 |
NIH Device Record Key | 90f0fe6e-b7c9-4e1f-be17-3e2e9ee8943d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CIRCLED |
Version Model Number | CIRCLED /D |
Catalog Number | 110001 |
Company DUNS | 435188508 |
Company Name | ACEM SPA |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08050705890019 [Primary] |
KZF | Device, Medical Examination, Ac Powered |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2020-03-20 |
Device Publish Date | 2020-01-31 |
08050705890033 | CIRCLED 3/5 DIOPTERS TROLLEY |
08050705890026 | CIRCLED 3/5 DIOPTERS WALL |
08050705890019 | CIRCLED 3/5 DIOPTERS TABLE |
08050705890002 | CIRCLED 3/5 DIOPTERS RAIL |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CIRCLED 85820074 4430024 Live/Registered |
Qintar Technologies, Inc. 2013-01-10 |