2ml ~ 3ml capacity amber open sterile vials, 2ml 3ml RTU vials (ready to use), approx 15.95mm x 35mm, small count alveolar nested tray of 100 vials.
3rd party sterility and endotoxin testing is performed by a USA accredited laboratory.
No minimum purchase and worldwide delivery.
Design allows for manual vial filling only.
Catalog VA1002NC105
We do not sell customer sales data.
Orders are generally shipped within 1 business day after receipt of payment, Monday through Friday.
Sterile items cannot be returned. All other items must receive a return authorization in writing.
Formulated for laboratories and compounding pharmacies that demand consistency, these amber sterile vials are close to an ISO 2R size ( 15.95mm x 35mm VS an ISO 2R at 16x35mm), manufactured from USP Type I borosilicate glass for superior chemical resistance and protection against light-sensitive degradation.
Each vial measures 15.95mm x 35mm, closely matching an ISO 2R 16x35mm specifications, to help achieve precise fill-volume and closure compatibility.
Small Count Nested Tray Packaging — Built for Safe Transit: Every vial ships in a protection nested sleeve tray holding 100 vials per tray. Individual cavities keep glass-to-glass contact to zero during shipping and handling, virtually eliminating chips, scuffs, and cosmetic damage before the vials ever reach your bench.
Designed only for manual filling only: Intended for manual aseptic filling only. Not validated or intended for use in automated robotic filling machinery.
The tray can act as a sterile vial rack in the cleanroom environment.
Right-Sized for Small-Batch Compounding - A 100-count tray is intentionally sized for smaller production runs, making these vials a practical fit for USP <797> compliance in Compounded Sterile Preparation (CSP) workflows — specifically batches requiring sterility testing at a final yield of 250 units or fewer. Order only what a given batch calls for, without breaking sterility assurance on a larger, unused case.
Full Quality Documentation Included - Each lot ships with complete third-party testing documentation: Sterility Testing and Endotoxin Testing report is performed by an independent, FDA-registered U.S. laboratory holding GMP, GLP, and GTP certifications, with ISO/IEC 17025 accreditation — giving you an added layer of quality assurance for regulated compounding and lab use.
Specific References
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