Primary Device ID | 00841132179949 |
NIH Device Record Key | 1ff612d5-35fd-43c8-93ba-928b82c13871 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Orthex Tool |
Version Model Number | PP460-45-100 |
Catalog Number | PP460-45-100 |
Company DUNS | 796416191 |
Company Name | ORTHOPEDIATRICS CORP. |
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 | false |
Device Combination Product | false |
Single Use | false |
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(574)268-6379 |
bsmith@orthopediatrics.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841132179949 [Primary] |
LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00841132179949]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-03-10 |
Device Publish Date | 2020-03-02 |
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