BD Microtainer® Quikheel™ Preemie Lancet 368100
GUDID 30382903681007
LANCET QUIKHEEL PINK 0.85MMX1.75MM
BECTON, DICKINSON AND COMPANY
Manual blood lancing device, single-use| Primary Device ID | 30382903681007 |
| NIH Device Record Key | e0f094bf-b854-4ebb-aa52-8fd49b2cb9ea |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BD Microtainer® Quikheel™ Preemie Lancet |
| Version Model Number | 368100 |
| Catalog Number | 368100 |
| 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 | 00382903681006 [Unit of Use] |
| GS1 | 30382903681007 [Package] Contains: 50382903681001 Package: Shelfpack [50 Units] In Commercial Distribution |
| GS1 | 50382903681001 [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 |
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| 00382904413583 - Male Urethral Collection Kit for BD ProbeTec™ (CT/GC) Qx Amplified DNA Assays | 2025-08-25 Swab Male Urethral Specimen Collection |
| 00382903059041 - BD SafetyGlide | 2025-08-07 SYRINGE 3ML LL W/NDL SFTYGLD 25X5/8 RB |
| 00382903059058 - BD SafetyGlide | 2025-08-07 SYRINGE 3ML LL W/NDL SFTYGLD 23X1 RB |
| 00382903059065 - BD SafetyGlide | 2025-08-07 SYRINGE 3ML LL W/NDL SFTYGLD 22X1-1/2 RB |
| 00382903059096 - BD SafetyGlide | 2025-08-07 SYR 3ML LL W/NDL SFTYGLD 21X1-1/2 RB TW |
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 |
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