Primary Device ID | 04049539102171 |
NIH Device Record Key | bc82368a-31cb-48f6-838a-d86f04418541 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | OPMI® Drapes |
Version Model Number | 326044-0000-000 |
Company DUNS | 342228620 |
Company Name | Carl Zeiss Meditec AG |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Height | 43 Inch |
Width | 19 Inch |
Height | 110 Centimeter |
Width | 49 Centimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04049539101174 [Primary] |
GS1 | 04049539101969 [Package] Contains: 04049539101174 Package: [15 Units] In Commercial Distribution |
GS1 | 04049539102171 [Package] Contains: 04049539101969 Package: [10 Units] In Commercial Distribution |
KKX | Drape, Surgical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-11-22 |
Device Publish Date | 2016-08-22 |
04049539101310 | 326084-0000-000 |
04049539102171 | 326044-0000-000 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
OPMI 73267838 1173004 Live/Registered |
Carl-Zeiss-Stiftung 1980-06-25 |