Primary Device ID | 00847538007787 |
NIH Device Record Key | d67f3352-4903-4264-93e8-3509eb67eaca |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Component Impactor |
Version Model Number | 10-016-400-1500 |
Catalog Number | 2011-03-037 |
Company DUNS | 079881212 |
Company Name | SYMMETRY MEDICAL INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00847538007787 [Primary] |
LXH | Orthopedic Manual Surgical Instrument |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00847538007787]
Moist Heat or Steam Sterilization
[00847538007787]
Moist Heat or Steam Sterilization
[00847538007787]
Moist Heat or Steam Sterilization
[00847538007787]
Moist Heat or Steam Sterilization
[00847538007787]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-05-25 |
Device Publish Date | 2022-05-17 |
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