Primary Device ID | 04049584032454 |
NIH Device Record Key | cd325796-85e4-4dc0-8e5b-02130cc5a162 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Lidstick |
Version Model Number | 77500 |
Company DUNS | 317138956 |
Company Name | OCULUS Optikgeräte Gesellschaft mit beschränkter Haftung |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04049584032454 [Primary] |
GS1 | 04049584032959 [Package] Package: Individual roll [100 Units] In Commercial Distribution |
GS1 | 04049584032966 [Package] Contains: 04049584032959 Package: Box [2 Units] In Commercial Distribution |
GS1 | 04049584032973 [Package] Contains: 04049584032966 Package: Shipper [16 Units] In Commercial Distribution |
HNI | Retractor, Ophthalmic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-06-26 |
Device Publish Date | 2023-06-16 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
LIDSTICK 98828383 not registered Live/Pending |
Alexander, Nicola 2024-10-30 |
LIDSTICK 88642264 not registered Live/Pending |
Novalash, Inc. 2019-10-04 |
LIDSTICK 79270426 not registered Live/Pending |
Oculus Optikgeräte GmbH 2019-08-22 |