Primary Device ID | 14953170337540 |
NIH Device Record Key | a9807a0f-65b2-4ee5-a3d5-438e9c0281f7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | THUNDERBEAT 5 mm, 45 cm, Front-actuated Grip |
Version Model Number | TB-0545FC |
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 |
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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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Device Issuing Agency | Device ID |
---|---|
GS1 | 04953170337543 [Primary] |
GS1 | 14953170337540 [Package] Contains: 04953170337543 Package: [5 Units] In Commercial Distribution |
KNS | Unit, electrosurgical, endoscopic (with or without accessories) |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-21 |