Primary Device ID | B2219001050051 |
NIH Device Record Key | f8e755e1-c414-4416-8df8-8e3dc3cc9ef6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EPIX Distal Screw 50.0mm x 5mm |
Version Model Number | 9001-05005 |
Catalog Number | 9001-05005 |
Company DUNS | 084913303 |
Company Name | Epix Orthopaedics 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 | 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 | +1(844)710-9105 |
epixortho@icloud.com | |
Phone | +1(844)710-9105 |
epixortho@icloud.com |
Length | 47.5 Millimeter |
Length | 47.5 Millimeter |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B2219001050051 [Primary] |
HSB | ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES |
Steralize Prior To Use | true |
Device Is Sterile | false |
[B2219001050051]
Moist Heat or Steam Sterilization
[B2219001050051]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-03-13 |
Device Publish Date | 2019-03-05 |
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