| Primary Device ID | 10850055961149 |
| NIH Device Record Key | 3c8ea938-986c-419d-833c-6bc40fa1e80a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Loocid BCP |
| Version Model Number | UNI-BB-30-R |
| Company DUNS | 118930609 |
| Company Name | LOOCID LLC |
| Device Count | 5 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 |
| Phone | +1(833)865-5999 |
| info@loocid.com | |
| Phone | +1(833)865-5999 |
| info@loocid.com | |
| Phone | +1(833)865-5999 |
| info@loocid.com | |
| Phone | +1(833)865-5999 |
| info@loocid.com | |
| Phone | +1(833)865-5999 |
| info@loocid.com | |
| Phone | +1(833)865-5999 |
| info@loocid.com | |
| Phone | +1(833)865-5999 |
| info@loocid.com | |
| Phone | +1(833)865-5999 |
| info@loocid.com | |
| Phone | +1(833)865-5999 |
| info@loocid.com | |
| Phone | +1(833)865-5999 |
| info@loocid.com | |
| Phone | +1(833)865-5999 |
| info@loocid.com | |
| Phone | +1(833)865-5999 |
| info@loocid.com | |
| Phone | +1(833)865-5999 |
| info@loocid.com | |
| Phone | +1(833)865-5999 |
| info@loocid.com | |
| Phone | +1(833)865-5999 |
| info@loocid.com |
| Outer Diameter | 3 Millimeter |
| Outer Diameter | 3 Millimeter |
| Outer Diameter | 3 Millimeter |
| Outer Diameter | 3 Millimeter |
| Outer Diameter | 3 Millimeter |
| Outer Diameter | 3 Millimeter |
| Outer Diameter | 3 Millimeter |
| Outer Diameter | 3 Millimeter |
| Outer Diameter | 3 Millimeter |
| Outer Diameter | 3 Millimeter |
| Outer Diameter | 3 Millimeter |
| Outer Diameter | 3 Millimeter |
| Outer Diameter | 3 Millimeter |
| Outer Diameter | 3 Millimeter |
| Outer Diameter | 3 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00850051972975 [Primary] |
| GS1 | 10850055961149 [Unit of Use] |
| DZA | DRILL, DENTAL, INTRAORAL |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[10850055961149]
Moist Heat or Steam Sterilization
[10850055961149]
Moist Heat or Steam Sterilization
[10850055961149]
Moist Heat or Steam Sterilization
[10850055961149]
Moist Heat or Steam Sterilization
[10850055961149]
Moist Heat or Steam Sterilization
[10850055961149]
Moist Heat or Steam Sterilization
[10850055961149]
Moist Heat or Steam Sterilization
[10850055961149]
Moist Heat or Steam Sterilization
[10850055961149]
Moist Heat or Steam Sterilization
[10850055961149]
Moist Heat or Steam Sterilization
[10850055961149]
Moist Heat or Steam Sterilization
[10850055961149]
Moist Heat or Steam Sterilization
[10850055961149]
Moist Heat or Steam Sterilization
[10850055961149]
Moist Heat or Steam Sterilization
[10850055961149]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-04-05 |
| Device Publish Date | 2024-03-28 |