Primary Device ID | 04049539101242 |
NIH Device Record Key | 18bc6f00-493e-45c8-ac3f-8767a5a55198 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | OPMI® Drapes sterile |
Version Model Number | 306079-0000-000 |
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 | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Height | 59 Inch |
Width | 20 Inch |
Height | 150 Centimeter |
Width | 51 Centimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04049539101242 [Primary] |
GS1 | 04049539102034 [Package] Package: [10 Units] In Commercial Distribution |
GS1 | 04049539102249 [Package] Contains: 04049539102034 Package: [6 Units] In Commercial Distribution |
KKX | Drape, Surgical |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-08-22 |
04049539102294 | 326082-0000-000 |
04049539101280 | 326018-0000-000 |
04049539101273 | 326013-0000-000 |
04049539101266 | 326009-0000-000 |
04049539102256 | 326005-0000-000 |
04049539101242 | 306079-0000-000 |
04049539101235 | 306075-0000-000 |
04049539102225 | 306073-0000-000 |
04049539102218 | 306071-0000-000 |
04049539102201 | 306070-0000-000 |
04049539102195 | 306026-0000-000 |
04049539101181 | 306025-0000-000 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
OPMI 73267838 1173004 Live/Registered |
Carl-Zeiss-Stiftung 1980-06-25 |