BD #309578 - Syringe 3cc LL 20gx1" w/ Detachable PrecisionGlide Needle 100/Bx, 8 BX/CA

BD #309578 - Syringe 3cc LL 20gx1
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Product Description

BD Part #309578 - Syringe 3cc LL 20gx1" w/ Detachable PrecisionGlide Needle 100/Bx, 8 BX/CA

309578 - 3 mL BD Luer-Lok Syringe with attached needle 20 G x 1 in., sterile, single use

3cc, 20 G x 1 in.", Standard Syringe with Needle

3mL Luer-Lok Syringe with 20 G x 1 in." PrecisionGlide Needle Combination. Regular bevel, regular wall. Detachable needle. World's sharpest needle is combined with BD's clear barrel featuring bold scale. Syringes have positive plunger rod stop and tapered plunger rod design.

BD conventional syringes are available with and without an attached needle. BD syringe-needle combinations feature a clear barrel with a bold scale. Disposable syringes with a BD Luer-Lok tip, luer slip tip or eccentric luer slip tip can be fitted with either a conventional needle or safety needle.

Key Product Features

Detachable NeedleProduct has a detachable needle
Hub ColorYellow
Hub MaterialPolypropylene
Hub TypeLuer
Needle Gauge20 G
Needle Gauge (m)0.90 mm
Needle Length (in.)1 in.
Needle Length (m)25.40 mm
Needle Tip TypeRegular
Needle TypeHypodermic
Needle Wall TypeRegular
Priming Volume0.086 mL
Pyrogen FreeProduct is pyrogen free
Syringe Tip OrientationConcentric
Syringe Tip TypeBD Luer-Lok
Syringe Scale0.1 ml graduations
Total Shelf Life1825
SterileSterilized product
Volumetric Accuracy+/- 5% *for 1ml or smaller,accuracy below 0.2ml is+/- 0.07ml
Sterilization MethodEO, Radiation
BPA FreeNot made with BPA
DEHP FreeNot made with DEHP
Latex StatementNot made with natural rubber latex
PVC FreeNot made with PVC
DisposableDisposable product
Single UseProduct is for single use only

Regulatory Compliance and Quality System

BD Products comply with the regulatory requirements of the region in which these are sold and manufactured.

Sterility

All products which are labeled as #sterile# and released for sale by BD are certified to be sterile as long as the package is unopened and undamaged. For those products labeled #sterile fluid path#, only the fluid path is sterile.

This product is primarily sterilized via E-beam. Sterilization cycle development/validation is performed to 10-6 SAL in accordance with current ISO 11137 guidelines.

Pyrogenicity

All products which are labeled as non-pyrogenic and released for sale by BD have been tested per United States Pharmacopeia (USP) chapter 85 - Bacterial Endotoxins Test and meets limits as specified in chapter 161- Transfusion and Infusion Assemblies and Similar Medical Devices.

Biocompatability

This product has been evaluated in accordance with ISO 10993 "Biological Evaluation of Medical Devices", and complies with all relevant sections.

Quality Control Testing and Release

Representative production samples are collected and inspected in accordance with current applicable product specifications. Inspection records are reviewed and signed off by qualified personnel for product release. The released devices meet applicable BD product specifications.

Device Characteristics

What MRI safety information does the labeling contain?Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)No
Device labeled as "Not made with natural rubber latex"No
For Single-UseYes
Prescription Use (Rx)Yes
Over the Counter (OTC)No
KitNo
Combination ProductNo
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)No

Product Packaging Information

Packaging LevelShelfpackEachCase
Quantity1001800
Length210.0 mm419.0 mm
Width188 mm375.0 mm
Height170 mm330.0 mm
Weight672.5 g6.724 g5.38 kg