Primary Device ID | B2213212095111 |
NIH Device Record Key | 90eb0f82-348d-4ba7-ba5b-654adc4d7666 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EPIX Lag Screw 95mm x 11mm |
Version Model Number | 3212-09511 |
Catalog Number | 3212-09511 |
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 | 95 Millimeter |
Length | 95 Millimeter |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B2213212095111 [Primary] |
HSB | ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES |
Steralize Prior To Use | true |
Device Is Sterile | false |
[B2213212095111]
Moist Heat or Steam Sterilization
[B2213212095111]
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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