Primary Device ID | 00850041090122 |
NIH Device Record Key | 830b0472-4036-4784-8aea-1210c1fb5d48 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ACCURUN® |
Version Model Number | 2020-0185 |
Company DUNS | 106267123 |
Company Name | Lgc Clinical Diagnostics, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | true |
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 | 00850041090122 [Primary] |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-08-12 |
Device Publish Date | 2024-08-02 |
00850041090047 | ACCURUN Babesia Molecular Controls Kit |
00860006589790 | 0505-0300 |
00860006589776 | 2000-0079 |
00860006589707 | 2000-0080 |
00850041090122 | 2020-0185 |
00850041090115 | 2020-0164 |
00850041090108 | 2000-0107 |
00850041090092 | 2000-0106 |
00850041090085 | 2010-0026 |
00850041090078 | 2010-0025 |
00850041090061 | 2000-0105 |
00850041090054 | 2020-0162 |
00850041090030 | 2000-0102 |
00850041090023 | 2015-0240 |
00850041090016 | 2010-0023 |
00850041090009 | 2000-0101 |
00816784021007 | 2000-0071 |
00816784020864 | 0505-0220 |
00816784020741 | 2000-0079 |
00816784020734 | 0505-0242 |
00816784020086 | 0505-0227 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ACCURUN 90099182 not registered Live/Pending |
AccuRun LLC 2020-08-07 |
ACCURUN 75198245 2109153 Live/Registered |
SERACARE LIFE SCIENCES, INC. 1996-11-04 |