Primary Device ID | 14953170244060 |
NIH Device Record Key | 4cdcd933-9ba9-430f-822d-b811652f4e4d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Single Use Retrieval Basket V |
Version Model Number | FG-V432P |
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 | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04953170244063 [Primary] |
GS1 | 14953170244060 [Package] Contains: 04953170244063 Package: [1 Units] In Commercial Distribution |
OCZ | Endoscopic grasping/cutting instrument, non-powered |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-05-06 |
Device Publish Date | 2016-09-21 |
14953170244060 | Single Use Retrieval Basket V |
14953170244053 | Single Use Retrieval Basket V |
14953170244046 | Single Use Retrieval Basket V |
14953170244039 | Single Use Retrieval Basket V |