Primary Device ID | 00192029028292 |
NIH Device Record Key | 10fc1caa-b0a8-4c16-a900-b3b2e803e097 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Hook Pin |
Version Model Number | 207-311 |
Company DUNS | 005432299 |
Company Name | TP ORTHODONTICS 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 | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | +1(219)785-2591 |
nicholas.smith@tportho.com | |
Phone | +1(219)785-2591 |
nicholas.smith@tportho.com | |
Phone | +1(219)785-2591 |
nicholas.smith@tportho.com | |
Phone | +1(219)785-2591 |
nicholas.smith@tportho.com | |
Phone | +1(219)785-2591 |
nicholas.smith@tportho.com | |
Phone | +1(219)785-2591 |
nicholas.smith@tportho.com | |
Phone | +1(219)785-2591 |
nicholas.smith@tportho.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00192029028292 [Primary] |
ECN | CLAMP, WIRE, ORTHODONTIC |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-05-17 |
Device Publish Date | 2022-05-09 |
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