Primary Device ID | 14953170183796 |
NIH Device Record Key | 9eef8a3d-2b7e-487a-bca4-65471df012ff |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Single Use Cannula V |
Version Model Number | PR-V427Q |
Company DUNS | 711789789 |
Company Name | OLYMPUS MEDICAL SYSTEMS CORP. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)401-1086 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04953170183799 [Primary] |
GS1 | 14953170183796 [Package] Contains: 04953170183799 Package: [1 Units] In Commercial Distribution |
ODD | Endoscopic retrograde cholangiopancreatography (ERCP) cannula |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-21 |
14953170183833 | Single Use Cannula V |
14953170183819 | PR-V434Q |
14953170183796 | Single Use Cannula V |
14953170183772 | Single Use Cannula V |
14953170183758 | Single Use Cannula V |
14953170183734 | PR-V416Q |
14953170183710 | Single Use Cannula V |
14953170183697 | Single Use Cannula V |
14953170183635 | PR-V227Q |
14953170183611 | PR-V220Q |
14953170183574 | PR-V216Q |
14953170183550 | PR-V214Q |