Primary Device ID | 10190707088252 |
NIH Device Record Key | a35d2d10-e54a-4069-af68-d37255579c38 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Carriere D-LX |
Version Model Number | 103-191C |
Company DUNS | 062165188 |
Company Name | ORTHO ORGANIZERS, INC. |
Device Count | 10 |
DM Exempt | true |
Pre-market Exempt | true |
MRI Safety Status | MR Unsafe |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00190707088255 [Primary] |
GS1 | 10190707088252 [Unit of Use] |
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 | 2025-06-26 |
Device Publish Date | 2025-06-18 |
10190707088498 | 019x025 Carriere D-LX CuNitanium 35° w/ EZ Stops Single Pack(10) |
10190707088467 | 017x025 Carriere D-LX CuNitanium 35° w/ EZ Stops Single Pack(10) |
10190707088351 | 014x025 Carriere D-LX CuNitanium 27° w/ EZ Stops Single Pack(10) |
10190707088283 | 014 Carriere D-LX Cu Nitanium 27° w/ EZ Stops Single Pack (10) |
10190707088252 | 013 Carriere D-LX Cu Nitanium 27° w/ EZ Stops Single Pack (10) |