Primary Device ID | B064XM38113571 |
NIH Device Record Key | 356d448f-1b28-4f2f-8a60-1131a00b1d0c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 38mm x 30mm x 12° ALIF Rasp Kit 11, 13, 15, 17mm Heights |
Version Model Number | XM-381-1357 |
Company DUNS | 079282130 |
Company Name | XENCO MEDICAL LLC |
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 | true |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B064XM38113571 [Primary] |
Steralize Prior To Use | true |
Device Is Sterile | true |
[B064XM38113571]
Radiation Sterilization
[B064XM38113571]
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[B064XM38113571]
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[B064XM38113571]
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[B064XM38113571]
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[B064XM38113571]
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[B064XM38113571]
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[B064XM38113571]
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[B064XM38113571]
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[B064XM38113571]
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[B064XM38113571]
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[B064XM38113571]
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[B064XM38113571]
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[B064XM38113571]
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[B064XM38113571]
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[B064XM38113571]
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[B064XM38113571]
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[B064XM38113571]
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[B064XM38113571]
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[B064XM38113571]
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[B064XM38113571]
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[B064XM38113571]
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[B064XM38113571]
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[B064XM38113571]
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[B064XM38113571]
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[B064XM38113571]
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[B064XM38113571]
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[B064XM38113571]
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[B064XM38113571]
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[B064XM38113571]
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Radiation Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-04-06 |
Device Publish Date | 2015-10-28 |
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