Primary Device ID | 15420045504981 |
NIH Device Record Key | 92a471c6-d42b-47d8-90c4-793cf414c0dc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EVIVA_1210-20 |
Version Model Number | EVIVA_1210-20 |
Catalog Number | EVIVA_1210-20 |
Company DUNS | 018925968 |
Company Name | Hologic, Inc. |
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 | 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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 15420045504981 [Primary] |
GS1 | 25420045504988 [Package] Package: BOX [5 Units] In Commercial Distribution |
GS1 | 35420045504985 [Package] Package: BOX [5 Units] In Commercial Distribution |
KNW | INSTRUMENT, BIOPSY |
Steralize Prior To Use | true |
Device Is Sterile | false |
[15420045504981]
Radiation Sterilization
[15420045504981]
Radiation Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2018-07-12 |
Device Publish Date | 2016-07-26 |
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