Primary Device ID | 00850051972074 |
NIH Device Record Key | b9193d4d-504a-4f59-9f4f-a897e20f4c40 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Loocid BCP |
Version Model Number | NBR-S-35 |
Company DUNS | 118930609 |
Company Name | LOOCID LLC |
Device Count | 1 |
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 | 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 | 3.5 Millimeter |
Outer Diameter | 3.5 Millimeter |
Outer Diameter | 3.5 Millimeter |
Outer Diameter | 3.5 Millimeter |
Outer Diameter | 3.5 Millimeter |
Outer Diameter | 3.5 Millimeter |
Outer Diameter | 3.5 Millimeter |
Outer Diameter | 3.5 Millimeter |
Outer Diameter | 3.5 Millimeter |
Outer Diameter | 3.5 Millimeter |
Outer Diameter | 3.5 Millimeter |
Outer Diameter | 3.5 Millimeter |
Outer Diameter | 3.5 Millimeter |
Outer Diameter | 3.5 Millimeter |
Outer Diameter | 3.5 Millimeter |
Special Storage Condition, Specify | Between 0 and 0 *Keep in dry conditions |
Special Storage Condition, Specify | Between 0 and 0 *Keep in dry conditions |
Special Storage Condition, Specify | Between 0 and 0 *Keep in dry conditions |
Special Storage Condition, Specify | Between 0 and 0 *Keep in dry conditions |
Special Storage Condition, Specify | Between 0 and 0 *Keep in dry conditions |
Special Storage Condition, Specify | Between 0 and 0 *Keep in dry conditions |
Special Storage Condition, Specify | Between 0 and 0 *Keep in dry conditions |
Special Storage Condition, Specify | Between 0 and 0 *Keep in dry conditions |
Special Storage Condition, Specify | Between 0 and 0 *Keep in dry conditions |
Special Storage Condition, Specify | Between 0 and 0 *Keep in dry conditions |
Special Storage Condition, Specify | Between 0 and 0 *Keep in dry conditions |
Special Storage Condition, Specify | Between 0 and 0 *Keep in dry conditions |
Special Storage Condition, Specify | Between 0 and 0 *Keep in dry conditions |
Special Storage Condition, Specify | Between 0 and 0 *Keep in dry conditions |
Special Storage Condition, Specify | Between 0 and 0 *Keep in dry conditions |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850051972074 [Primary] |
DZA | DRILL, DENTAL, INTRAORAL |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00850051972074]
Moist Heat or Steam Sterilization
[00850051972074]
Moist Heat or Steam Sterilization
[00850051972074]
Moist Heat or Steam Sterilization
[00850051972074]
Moist Heat or Steam Sterilization
[00850051972074]
Moist Heat or Steam Sterilization
[00850051972074]
Moist Heat or Steam Sterilization
[00850051972074]
Moist Heat or Steam Sterilization
[00850051972074]
Moist Heat or Steam Sterilization
[00850051972074]
Moist Heat or Steam Sterilization
[00850051972074]
Moist Heat or Steam Sterilization
[00850051972074]
Moist Heat or Steam Sterilization
[00850051972074]
Moist Heat or Steam Sterilization
[00850051972074]
Moist Heat or Steam Sterilization
[00850051972074]
Moist Heat or Steam Sterilization
[00850051972074]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-03-12 |
Device Publish Date | 2024-03-04 |