STERiJECT
Contact TSK

STERiJECT™ Ophthalmic VLDS Needle

VLDS: Ophthalmic Low Dead Space

Our ophthalmic-cleared, low-dead-space needle, built to give back what a standard hub holds onto.

FDA 510(k) cleared · U.S. Intravitreal USP <789> 0.2 EU per device 360° threading Enlarged lumen

VLDS is TSK's low-dead-space needle line, and the only one with FDA 510(k) clearance for ophthalmic use in the United States. A low-dead-space hub, ophthalmic cannula and secure luer-lock connection work together, with each production lot tested for USP <789> particulate compliance and to a bacterial endotoxin limit of 0.2 EU per device. Availability varies by product code and region.

STERiJECT Ophthalmic Low Dead Space Needle and product packaging

STERiJECT™ Ophthalmic Low Dead Space Needle and product packaging.

0.005 mLResidual volume · tested VLDS hub1,2
0.042 mLTested conventional hub, same method
0.2 EUBacterial endotoxin limit per device
30 – 34GGauges · 4 · 9 · 13 mm lengths

Engineering

Design features

  • 01Low-dead-space hub

    Designed to reduce medication retained at the needle connection after delivery. In bench testing, the VLDS hub retained 0.005 mL versus 0.042 mL for a tested conventional hub.

  • 02Extra-thin-wall cannula & enlarged lumen

    An enlarged internal diameter supports flow through fine-gauge configurations and can reduce the force required to move fluid through the cannula.

  • 03360° external threading

    Full circumferential engagement with a compatible luer-lock syringe for a secure connection.

  • 04Hard polycarbonate hub

    Rigid construction that resists hub deformation and needle movement under load.

  • 05Sharp lancet bevel

    Engineered for low penetration force; a proprietary coating supports glide and reduces vitreous drag.

  • 06Ophthalmic quality pathway

    Lot testing includes USP <789> particulate requirements and a bacterial endotoxin limit of 0.2 EU per device.

Externally threaded VLDS hub and ophthalmic cannula

Externally threaded VLDS hub and ophthalmic cannula.

Quality

Ophthalmic quality controls

Every VLDS lot passes the same three checks before it ships.

  • Particulate control

    Tested before release for USP <789> compliance.

  • Silicone oil management

    Construction and handling assessed as a complete delivery system to manage droplet release.

  • Bacterial endotoxin testing

    Tested to a limit of 0.2 EU per device.

Product data

Configurations

Product type
Disposable ophthalmic sharp needle for intravitreal use
Materials
Hard polymer hub, stainless-steel cannula
Connection
Externally threaded luer-lock hub
Available sizes
30G, 32G, 33G and 34G/0.20 mm; 4, 9 and 13 mm, depending on product code
Cannula options
Regular-wall and extra-/ultra-thin-wall, depending on code
U.S. regulatory status
FDA 510(k)-cleared for ophthalmic use
Product codeLumenGaugeLength
VLDS-02009-050Regular Wall34G (0.20 mm)9mm (3/8 inch)
VLDS-33009-050Regular Wall33G9mm (3/8 inch)
VLDS-32013-050Regular Wall32G13mm (1/2 inch)
VLDS-32009-050Regular Wall32G9mm (3/8 inch)
VLDS-32004-050Regular Wall32G4mm (5/32 inch)
VLDS-30013E-050Ultra Thin Wall30G13mm (1/2 inch)

Available U.S. configurations. Product codes, packaging and availability vary by region.

Performance evidence

Bench results

  • Residual volume — 0.005 mL for the tested VLDS hub versus 0.042 mL for the tested conventional hub.

  • Penetration force — 33G STERiJECT ophthalmic needle showed a penetration force 0.014 N lower than the tested comparator.

  • Rigidity and flow — the tested 33G configuration showed a shorter bending distance and higher flow than its comparator.

  • Connection strength — 50 N pop-off force for the tested 34G configuration versus 39 N for its comparator.

These bench comparisons apply to the tested sizes, methods and comparators; they are not peer-reviewed clinical outcomes.

TSK online shop

View VLDS in the TSK online shop Review product details and available configurations.