Primary Device ID | 07290109141725 |
NIH Device Record Key | bea8b9b7-8b72-4ac7-85fc-f40ad7689e6c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MicroSlad™ 719 Lens Slide 350 mm |
Version Model Number | 19104 |
Company DUNS | 600166524 |
Company Name | LUMENIS LTD. |
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 | 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 | 408-764-3000 |
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Phone | 408-764-3000 |
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Phone | 408-764-3000 |
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Phone | 408-764-3000 |
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Phone | 408-764-3000 |
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Phone | 408-764-3000 |
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Phone | 408-764-3000 |
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Phone | 408-764-3000 |
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Phone | 408-764-3000 |
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Phone | 408-764-3000 |
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Phone | 408-764-3000 |
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Phone | 408-764-3000 |
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Phone | 408-764-3000 |
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Phone | 408-764-3000 |
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Phone | 408-764-3000 |
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Phone | 408-764-3000 |
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Phone | 408-764-3000 |
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Phone | 408-764-3000 |
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Phone | 408-764-3000 |
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Phone | 408-764-3000 |
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Phone | 408-764-3000 |
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Phone | 408-764-3000 |
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Phone | 408-764-3000 |
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Phone | 408-764-3000 |
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Phone | 408-764-3000 |
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Phone | 408-764-3000 |
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Phone | 408-764-3000 |
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Phone | 408-764-3000 |
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Phone | 408-764-3000 |
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Phone | 408-764-3000 |
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Phone | 408-764-3000 |
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Phone | 408-764-3000 |
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Device Issuing Agency | Device ID |
---|---|
GS1 | 07290109141725 [Primary] |
GEX | Powered Laser Surgical Instrument |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-11-26 |
Device Publish Date | 2016-09-12 |
07290109141725 | 19104 |
07290109147017 | 19104 |