Primary Device ID | 14953170062237 |
NIH Device Record Key | d9e03ec5-a8cd-448a-820b-e37b1a94ef6e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CURETTE |
Version Model Number | CC-4CR-1 |
Company DUNS | 711789789 |
Company Name | OLYMPUS MEDICAL SYSTEMS CORP. |
Device Count | 1 |
DM Exempt | true |
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 | 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 | |
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 | |
Phone | +1(800)401-1086 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04953170062230 [Primary] |
GS1 | 14953170062237 [Package] Contains: 04953170062230 Package: [1 Units] In Commercial Distribution |
EOQ | BRONCHOSCOPE (FLEXIBLE OR RIGID) |
Steralize Prior To Use | true |
Device Is Sterile | false |
[14953170062237]
Moist Heat or Steam Sterilization
[14953170062237]
Moist Heat or Steam Sterilization
[14953170062237]
Moist Heat or Steam Sterilization
[14953170062237]
Moist Heat or Steam Sterilization
[14953170062237]
Moist Heat or Steam Sterilization
[14953170062237]
Moist Heat or Steam Sterilization
[14953170062237]
Moist Heat or Steam Sterilization
[14953170062237]
Moist Heat or Steam Sterilization
[14953170062237]
Moist Heat or Steam Sterilization
[14953170062237]
Moist Heat or Steam Sterilization
[14953170062237]
Moist Heat or Steam Sterilization
[14953170062237]
Moist Heat or Steam Sterilization
[14953170062237]
Moist Heat or Steam Sterilization
[14953170062237]
Moist Heat or Steam Sterilization
[14953170062237]
Moist Heat or Steam Sterilization
[14953170062237]
Moist Heat or Steam Sterilization
[14953170062237]
Moist Heat or Steam Sterilization
[14953170062237]
Moist Heat or Steam Sterilization
[14953170062237]
Moist Heat or Steam Sterilization
[14953170062237]
Moist Heat or Steam Sterilization
[14953170062237]
Moist Heat or Steam Sterilization
[14953170062237]
Moist Heat or Steam Sterilization
[14953170062237]
Moist Heat or Steam Sterilization
[14953170062237]
Moist Heat or Steam Sterilization
[14953170062237]
Moist Heat or Steam Sterilization
[14953170062237]
Moist Heat or Steam Sterilization
[14953170062237]
Moist Heat or Steam Sterilization
[14953170062237]
Moist Heat or Steam Sterilization
[14953170062237]
Moist Heat or Steam Sterilization
[14953170062237]
Moist Heat or Steam Sterilization
[14953170062237]
Moist Heat or Steam Sterilization
[14953170062237]
Moist Heat or Steam Sterilization
[14953170062237]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2018-10-08 |
Device Publish Date | 2016-09-21 |