BD Quincke Spinal NRFit
- Primary DI
- 30382904009244
- Brand
- BD Quincke Spinal NRFit
- Company
- BECTON, DICKINSON AND COMPANY
- Model
- 400924
- Catalog number
- 400924
- Device description
- BD® Quincke Spinal NRFit™ Needle, 27G x 3 1/2 in.
- Published
- 2022-07-01
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Product Codes#
| Code | Name |
|---|---|
| BSP | NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| BSP | Needle, Conduction, Anesthetic (W/Wo Introducer) | Anesthesiology | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K193131 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 30382904009244 | Package | GS1 | 25 | In Commercial Distribution |
| 50382904009248 | Package | GS1 | 4 | In Commercial Distribution |
| 00382904009243 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 30382904009244 | 30382904009244 | ||
| 50382904009248 | 50382904009248 | ||
| 00382904009243 | 00382904009243 | 382904009243 | 0382904009243 |
GMDN Terms#
| Term | Definition |
|---|---|
| Spinal needle, single-use | A sterile, sharp bevel-edged, hollow tubular metal instrument designed to deliver anaesthetic or analgesic agents intrathecally (in the space under the arachnoid membrane of the brain and spinal cord), withdraw a sample of cerebrospinal fluid (CSF), and/or assist introduction of an intrathecal catheter (e.g., lumboperitoneal shunt, spinal catheter). It is typically fenestrated, spring-tipped, and used for short-term administration; it is typically made of metal and plastic materials. This is a single-use device. |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Special Storage Condition, Specify | 0 | 0 | Room Temperature |
Sterilization Methods#
| Method |
|---|
Regulatory Flags#
- DUNS number
- 001292192
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- true
- Sterilization required before use
- false
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00382903840120 | BD Introsyte Autoguard | 384012 | 384012 | 2016-10-20 |
| 00382903840083 | BD Introsyte-N Autoguard, BD Instaflash | 384008 | 384008 | 2016-10-20 |
| 00382903840106 | BD Introsyte Autoguard | 384010 | 384010 | 2016-10-20 |
| 00382903840113 | BD Introsyte Autoguard | 384011 | 384011 | 2016-10-20 |
| 50382903840217 | BD Introsyte-N, BD Instaflash | 384021 | 384021 | 2016-10-20 |
| 50382903840309 | BD Introsyte | 384030 | 384030 | 2016-10-20 |
| 50382903840316 | BD Introsyte-N | 384031 | 384031 | 2016-10-20 |
| 50382903840408 | BD Introsyte | 384040 | 384040 | 2016-10-20 |
| 50382903840507 | BD Introsyte | 384050 | 384050 | 2016-10-20 |
| 00382904411268 | BD ProbeTec™ Chlamydia trachomatis (CT) Qx Amplified DNA Assay | 441126 | 441126 | 2018-05-25 |
| 00885403523437 | HemoSphere Alta | ALTAALL1 | ALTAALL1 | 2026-08-06 |
| 00885403523451 | HemoSphere Alta | ALTASR1 | ALTASR1 | 2026-08-06 |
| 00885403523475 | HemoSphere Alta | ALTACR1 | ALTACR1 | 2026-08-06 |
| 00382906718167 | Horizon | 671816 | 671816 | 2026-09-24 |
| 00382906718174 | Horizon | 671817 | 671817 | 2026-09-24 |
| 00382906718181 | Horizon | 671818 | 671818 | 2026-09-24 |
| 00382906718198 | Horizon | 671819 | 671819 | 2026-09-24 |
| 00382906718204 | Horizon | 671820 | 671820 | 2026-09-24 |
| 00382906718211 | Horizon | 671821 | 671821 | 2026-09-24 |
| 00382906718235 | Horizon | 671823 | 671823 | 2026-09-24 |
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