Primary Device ID | 04961333232208 |
NIH Device Record Key | 2a548897-aaf6-49f4-978d-ccd0f1f33ff1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ULTRASOUND BRONCHOSCOPE |
Version Model Number | EB-1970UK |
Company DUNS | 083211284 |
Company Name | PENTAX OF AMERICA, INC. |
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 | false |
Serial Number | true |
Manufacturing Date | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04961333232208 [Primary] |
EOQ | Bronchoscope (Flexible Or Rigid) |
Steralize Prior To Use | true |
Device Is Sterile | false |
[04961333232208]
Ethylene Oxide;High-level Disinfectant
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-04-06 |
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