Primary Device ID | 00192029016077 |
NIH Device Record Key | 669fc3a1-126b-4b95-a796-ab1a4ce42a11 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Reflex Coil Spring |
Version Model Number | 210-511 |
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 | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00192029016077 [Primary] |
DZC | 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 | 2021-03-23 |
Device Publish Date | 2021-03-15 |
00192029016091 | Double Coil Spring |
00192029016084 | Closed Coil Spring Heavy |
00192029016077 | Closed Coil Spring Medium |
00192029016060 | Closed Coil Spring Light |
00192029016053 | Double Coil Spring |
00192029016039 | Open Coil Spring Heavy Force |
00192029016022 | Aesthetic Open Coil Spring Medium Force |
00192029016015 | Open Coil Spring Medium Force |
00192029016008 | Open Coil Spring Light Force |