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BD 309626 Syringe 1cc LS 25 Gauge 5/8 Inch PrecisionGlide TB w/ Needle 800/CS

Product Description:

BD 309626 Syringe 1cc LS 25 Gauge 5/8 Inch PrecisionGlide TB w/ Needle 800/CS

blunt fill and filter needles C MPS HY 0816 0010 pds1cn

309626 – 1 mL BD Slip Tip Syringe with attached needle 25 G x 5/8 in., sterile, single use

309626 – 1 mL BD slip-tip syringe with 25 G x 5/8 in. BD Tuberculin Syringe with Detachable Needle, Slip Tip. (100/sp, 800/ca).

  • 1ml TB Syringe, Slip Tip with BD PrecisionGlide Needle 25 G x 5/8 in.
  • Sterile
  • Do Not Reuse
  • Do Not Reshield Used Needles
  • Not made with natural rubber latex
  • Not made with DEHP

30ml syringe

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 NeedleProduct has a detachable needle
Hub ColorBlue
Hub MaterialPolypropylene
Hub TypeLuer
Needle Gauge25 G
Needle Gauge (m)0.50 mm
Needle Length (in.)5/8 in.
Needle Length (m)15.88 mm
Needle Tip TypeRegular
Needle TypeHypodermic
Needle Wall TypeRegular
Priming Volume0.086 mL
Pyrogen FreeProduct is pyrogen free
Syringe Tip OrientationConcentric
Syringe Tip TypeSlip tip
Syringe Scale0.01 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.


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

Product Packaging Information

Packaging LevelShelfpackCaseEach
Length210.0 mm465.0 mm
Width178.0 mm295.0 mm
Height154.0 mm285.0 mm
Weight850.0 g6.8 kg8.5 g