BD Microtainer® QuikHeel™ Lancet 368101
GUDID 30382903681014
LANCET QUIKHEEL TEAL 1.0MMX2.5MM
BECTON, DICKINSON AND COMPANY
Manual blood lancing device, single-use| Primary Device ID | 30382903681014 |
| NIH Device Record Key | 71b76879-1a7e-4b31-b3e3-b8bf18865629 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BD Microtainer® QuikHeel™ Lancet |
| Version Model Number | 368101 |
| Catalog Number | 368101 |
| Company DUNS | 001292192 |
| Company Name | BECTON, DICKINSON AND COMPANY |
| Device Count | 200 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 | true |
| OTC Over-The-Counter | false |
Operating and Storage Conditions
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00382903681013 [Unit of Use] |
| GS1 | 30382903681014 [Package] Contains: 50382903681018 Package: Shelfpack [50 Units] In Commercial Distribution |
| GS1 | 50382903681018 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K223243
FDA Product Code
| FMK | Single use only blood lancet with an integral sharps injury prevention feature |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-03-23 |
| Device Publish Date | 2023-03-15 |
Devices Manufactured by BECTON, DICKINSON AND COMPANY
| 30382903059301 - SafetyGlide Insulin Syringe | 2025-05-19 SafetyGlide™ Insulin Syringes, U-100, 12.7mm, 29G, 1mL |
| 50382903059329 - SafetyGlide Insulin Syringe | 2025-05-19 SafetyGlide™ Insulin Syringes, U-100, 12.7mm, 29G, 0.5mL |
| 50382903059343 - SafetyGlide Insulin Syringe | 2025-05-19 SafetyGlide™ Insulin Syringes, U-100, 8mm, 30G, 0.5mL |
| 30382903059356 - SafetyGlide Insulin Syringe | 2025-05-19 SafetyGlide™ Insulin Syringes, U-100, 12.7mm, 29G, 0.3mL |
| 30382903059370 - SafetyGlide Insulin Syringe | 2025-05-19 SafetyGlide™ Insulin Syringes, U-100, 8mm, 31G, 0.3mL |
| 50382903284462 - SafetyGlide Insulin Syringe | 2025-05-19 SafetyGlide™ Insulin Syringes, U-100, 6mm, 31G, 1mL |
| 50382903284479 - SafetyGlide Insulin Syringe | 2025-05-19 SafetyGlide™ Insulin Syringes, U-100, 6mm, 31G, 0.5mL |
| 30382903284499 - SafetyGlide Insulin Syringe | 2025-05-19 SafetyGlide™ Insulin Syringes, U-100, 6mm, 31G, 0.3mL, 0.5 unit |
Trademark Results [BD Microtainer]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 BD MICROTAINER 78291051 2958371 Live/Registered |
Becton, Dickinson and Company 2003-08-22 |
 BD MICROTAINER 78279021 2912923 Live/Registered |
Becton, Dickinson and Company 2003-07-25 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.