Primary Device ID | 04953170214516 |
NIH Device Record Key | a35eddf8-05e3-49ac-b1a4-427e222253ed |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HDTV/SDTV monitor cable |
Version Model Number | MAJ-1462 |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)401-1086 |
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Phone | +1(800)401-1086 |
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Phone | +1(800)401-1086 |
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Phone | +1(800)401-1086 |
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Phone | +1(800)401-1086 |
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Phone | +1(800)401-1086 |
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Phone | +1(800)401-1086 |
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Phone | +1(800)401-1086 |
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Phone | +1(800)401-1086 |
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Phone | +1(800)401-1086 |
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Phone | +1(800)401-1086 |
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Phone | +1(800)401-1086 |
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Phone | +1(800)401-1086 |
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Phone | +1(800)401-1086 |
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Phone | +1(800)401-1086 |
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Phone | +1(800)401-1086 |
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Phone | +1(800)401-1086 |
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Phone | +1(800)401-1086 |
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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 |
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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 | |
Phone | +1(800)401-1086 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04953170214516 [Primary] |
FDF | Colonoscope and accessories, flexible/rigid |
NWB | Endoscope, accessories, narrow band spectrum |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-21 |