Primary Device ID | 14953170309158 |
NIH Device Record Key | 6ec62f9f-6d55-4a79-8463-87c71758ab27 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Single Use Aspiration Needle NA-220H/230H |
Version Model Number | NA-220H-8022 |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04953170309151 [Primary] |
GS1 | 14953170309158 [Package] Contains: 04953170309151 Package: [1 Units] In Commercial Distribution |
FCG | Biopsy needle |
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 |
14953170309233 | NA-230H-8022 |
14953170309219 | Single Use Aspiration Needle NA-220H/230H |
14953170309158 | NA-220H-8022 |
14953170309134 | Single Use Aspiration Needle NA-220H/230H |
14953170309110 | NA-220H-8019 |
14953170309097 | Single Use Aspiration Needle NA-220H/230H |