Primary Device ID | E0HM79BTXPR1 |
NIH Device Record Key | 4043e6ca-7ad4-4913-9cb1-058706cc2414 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Screw System TX Professional |
Version Model Number | BTXPR |
Catalog Number | BTXPR |
Company DUNS | 318034329 |
Company Name | Hager & Meisinger Gesellschaft mit beschränkter Haftung |
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 | 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 (303) 268-5400 |
info@meisingerusa.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | E0HM79BTXPR1 [Primary] |
HIBCC | E0HM79BTXPR9 [Previous] |
DZL | Screw, Fixation, Intraosseous |
Steralize Prior To Use | true |
Device Is Sterile | false |
[E0HM79BTXPR1]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-02-15 |
Device Publish Date | 2015-07-10 |
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