Primary Device ID | 04953170078361 |
NIH Device Record Key | 415f7096-8953-4646-a16c-6e49770dfc40 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | P CORD |
Version Model Number | MAJ-814 |
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 |
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 |
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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 |
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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 | |
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 | 04953170078361 [Primary] |
GEI | ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES |
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 |
04953170078361 | MAJ-814 |
04953170025693 | MAJ-003 P-CORD FOR UES-20/ PSD -20 |