




Gerresheimer 2R / 2 mL Amber Sterile Vials – ISO Standard Type I
Items must be purchased in nests of 120 units.
The 2 mL (2R) Amber Gerresheimer RTF® Sterile Vial, crafted from Type I Borosilicate Gx® Elite glass, sets the benchmark for sterile compounding. Designed to protect light-sensitive formulations, these vials undergo washing, depyrogenation, sterilization (ETO or VHP), and RTF® cleanroom packaging to ensure uncompromised sterility and safety.
Delivered in EZ-fill® nest & tub packaging, these vials prevent glass-to-glass contact, reduce breakage risk, and streamline aseptic handling in 503A/503B pharmacies and biopharma compounding environments. With Gx® Elite glass durability, cosmetic perfection, and regulatory compliance, they provide unmatched reliability for small-volume sterile drug preparation.
1 Nest & Tub = 120 units; 2 packs = 240 units (10 less than a complete 250-unit batch). These vials provide nearly a full 250-unit batch while minimizing glass-to-glass contact.
Relevant Industries
• Sterile Compounding Pharmacies (503A / 503B)
• Biopharmaceutical Manufacturing
• Clinical Research & Fill-Finish Facilities
• Vaccine and Biologics Production
Applications
• Aseptic preparation of sterile injectables
• Packaging of light-sensitive biologics (hormones, peptides, vaccines)
• Ready-to-Fill use in laminar flow isolators
• Batch sterile compounding requiring consistent vial quality
• Volume Capacity: 2 mL nominal (Brimful ~3.35 mL)
• Neck Finish: ISO 13 mm crimp neck
• Color: Amber – protects against UV/light degradation
• Material: ISO Standard Type I Borosilicate Glass (high chemical resistance)
• Packaging Configuration:
a) 1 Nest & Tub = 120 Vials
b) 2 Packs = 240 Vials (10 less than a 250-unit full batch)
• Sterilization Method: Ready-to-Fill (ETO or VHP)
• Dimensions: Ø 16.0 mm × H 35.0 mm (ISO 8362-1 Standard)
• Compatibility: Suitable with 13mm stoppers & seals
• Sterility Assurance: Compliant with USP <71> Sterility Tests
• Endotoxin Control: Meets USP <85> Bacterial Endotoxin requirements
• Residual Testing: Verified per ISO 10993-7 (ETO residuals)
• Glass Standards: Complies with USP <660>, Ph. Eur. 3.2.1, and JP for hydrolytic resistance
• Container Closure Integrity (CCI): Fully validated for sterile compounding workflows
• Defect Rate: Cosmetic defect reduction >90% with Gx® Elite glass inspection
• Documentation Supplied: Certificate of Conformance (CoC), Certificate of Analysis (CoA), Sterility & Endotoxin Reports
• Shelf Life: 3 years under recommended storage
Need technical support or help with a quote? Contact Us.
Component | Material | Properties / Features |
Transparent Peelable Polymer Lid | Opaque HDPE/PE |
|
Gx® Elite Glass Vials | Type I Borosilicate Glass |
|
Nest | Polypropylene Homopolymer |
|
Tyvek Stripes | HDPE |
|
Tub | High Impact Polypropylene Peterophasic Copolyme |
|
Boxes | Polypropylene |
|
Sterilization | ETO |
|