BD 309597 - Syringe 1cc LS 26gx5/8" SmartSlip Tip Dtch Ndl 100/Bx, 8 BX/CA


BD 309597 – Syringe 1cc LS 26gx5/8″ SmartSlip Tip Dtch Ndl 100/Bx, 8 BX/CA

309597 – 1 mL BD Slip Tip Syringe with attached needle 26 G x 5/8 in., Sterile, single use

1 mL BD Syringe/Needle Combination, Slip Tip

309597 – 1 mL BD slip-tip syringe with 26 G x 5/8 in. BD PrecisionGlide subcutaneous needle, regular bevel, regular wall. Detachable needle. (100/sp, 800/ca).

Luer slip tip

Our luer slip tip provides a friction-fit connection that requires you to push and twist the syringe tip into the needle hub.

Key Product Features

Detachable Needle Product has a detachable needle
Hub Color Tan
Hub Material Polypropylene
Hub Type Luer
Needle Gauge 26 G
Needle Gauge (m) 0.45 mm
Needle Length (in.) 5/8 in.
Needle Length (m) 15.88 mm
Needle Tip Type Regular
Needle Type Hypodermic
Needle Wall Type Regular
Priming Volume 0.086 mL
Pyrogen Free Product is pyrogen free
Syringe Tip Orientation Concentric
Syringe Tip Type Slip tip
Syringe Scale 0.01 mL graduations
Total Shelf Life 1825
Sterile Sterilized product
Sterilization Method EO, Radiation
BPA Free Not made with BPA
DEHP Free Not made with DEHP
Latex Statement Not made with natural rubber latex
PVC Free Not made with PVC
Disposable Disposable product
Single Use Product 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.


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.


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


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.

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-Use Yes
Prescription Use (Rx) Yes
Over the Counter (OTC) No
Kit No
Combination Product No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P) No

Product Packaging Information

Packaging Level Shelfpack Case Each
Quantity 100 800 1
Length 210.0 mm 419.0 mm
Width 178.0 mm 362.0 mm
Height 154.0 mm 305.0 mm
Weight 565.0 g 4.52 kg 5.65 g