BD Nexiva™ Diffusics™ Closed IV Catheter System 383589
GUDID 50382903835893
NEXIVA DIFFUSICS w/MaxZero 18G X 1.75 IN
BECTON, DICKINSON AND COMPANY
Peripheral intravenous cannula| Primary Device ID | 50382903835893 |
| NIH Device Record Key | 63d8f7e0-ed36-41a7-9f5b-e5e68cb8f3dc |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BD Nexiva™ Diffusics™ Closed IV Catheter System |
| Version Model Number | 383589 |
| Catalog Number | 383589 |
| Company DUNS | 124987988 |
| Company Name | BECTON, DICKINSON AND COMPANY |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| Human Cell/Tissue Product | false |
| Device Kit | true |
| Device Combination Product | false |
| Single Use | true |
| 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 |
Device Dimensions
| Length | 1.75 Inch |
| Total Volume | 0.6 Milliliter |
| Device Size Text, specify | 0 |
| Length | 1.75 Inch |
| Total Volume | 0.6 Milliliter |
| Device Size Text, specify | 0 |
| Length | 1.75 Inch |
| Total Volume | 0.6 Milliliter |
| Device Size Text, specify | 0 |
| Length | 1.75 Inch |
| Total Volume | 0.6 Milliliter |
| Device Size Text, specify | 0 |
| Length | 1.75 Inch |
| Total Volume | 0.6 Milliliter |
| Device Size Text, specify | 0 |
| Length | 1.75 Inch |
| Total Volume | 0.6 Milliliter |
| Device Size Text, specify | 0 |
| Length | 1.75 Inch |
| Total Volume | 0.6 Milliliter |
| Device Size Text, specify | 0 |
| Length | 1.75 Inch |
| Total Volume | 0.6 Milliliter |
| Device Size Text, specify | 0 |
| Length | 1.75 Inch |
| Total Volume | 0.6 Milliliter |
| Device Size Text, specify | 0 |
Operating and Storage Conditions
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Fragile, handle with care |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Fragile, handle with care |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Fragile, handle with care |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Fragile, handle with care |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Fragile, handle with care |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Fragile, handle with care |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Fragile, handle with care |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Fragile, handle with care |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Fragile, handle with care |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00382903835898 [Primary] |
| GS1 | 30382903835899 [Package] Contains: 00382903835898 Package: Shelfpack [20 Units] In Commercial Distribution |
| GS1 | 50382903835893 [Package] Contains: 30382903835899 Package: Case [4 Units] In Commercial Distribution |
FDA Product Code
| FOZ | Catheter, intravascular, therapeutic, short-term less than 30 days |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2025-09-17 |
| Device Publish Date | 2024-04-09 |
On-Brand Devices [BD Nexiva™ Diffusics™ Closed IV Catheter System]
| 30382903835967 | NEXIVA DIFFUSICS w/MaxZero 22G X 1.00 IN |
| 50382903835893 | NEXIVA DIFFUSICS w/MaxZero 18G X 1.75 IN |
Trademark Results [BD Nexiva]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 BD NEXIVA 78635118 3231147 Live/Registered |
Becton, Dickinson and Company 2005-05-23 |
 BD NEXIVA 78155329 not registered Dead/Abandoned |
Becton, Dickinson and Company 2002-08-19 |
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