Primary Device ID | 00190730007292 |
NIH Device Record Key | 05c6f20d-8cd0-4904-86c7-196b7dcc4a7d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Elastic Directors |
Version Model Number | 500-307 |
Company DUNS | 781772017 |
Company Name | ORTHO TECHNOLOGY, INC. |
Device Count | 1 |
DM Exempt | true |
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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00190730007292 [Primary] |
ECI | BAND, ELASTIC, ORTHODONTIC |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2017-09-27 |
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