Sellstrom S80231 Odyssey II Gamma Ray & Autoclave Clean Room Goggle Features
Sellstrom S80231 Odyssey II Clean Room Goggle is the designated eye protection specification for regulated pharmaceutical manufacturing, nuclear research, and ISO-classified sterile processing environments. Autoclave compatibility allows the goggle body to endure repeated steam sterilization cycles without structural degradation, seal compromise, or optical clarity loss. Gamma ray-resistant optical construction prevents lens yellowing and transmission degradation under sustained ionizing radiation exposure. Full ANSI/ISEA Z87.1+ impact compliance is retained across the product's complete sterilization-qualified service life.
Standard chemical goggles cannot survive autoclave sterilization — conventional PVC warps, elastic straps collapse, and optical coatings fail under thermal-steam exposure. Clean room environments additionally require non-particle-shedding materials certified for controlled contamination zones; standard goggle construction fails this requirement categorically. S80231 closes both specification gaps simultaneously within a single validated product. Procurement officers selecting PPE for ISO-classified clean rooms or nuclear handling environments must specify autoclave-rated goggle hardware as a baseline compliance requirement.
Goggle body materials are selected for compatibility across common laboratory sterilant formulations including peracetic acid, hydrogen peroxide vapor, and ethylene oxide processing environments. Post-autoclave inspection should confirm optical clarity, seal integrity, and lens retention before return to active service. Frame geometry supports over-the-glasses compatibility for corrective-lens personnel within clean room and sterile manufacturing environments. Storage must comply with your facility's ISO clean room material handling protocols between sterilization and deployment cycles.
Available Sizes and Configurations
| SKU | Configuration | Frame Material | Lens | Sterilization | Radiation Rating |
|---|---|---|---|---|---|
| SEL-S80231 | One Size Fits Most | Autoclave-Compatible Polymer | Clear Gamma Ray-Resistant Polycarbonate | Autoclave (Steam) Compatible | Gamma Ray Resistant Optics |
Technical Specifications
| Attribute | Detail |
|---|---|
| Product Type | Clean Room / Autoclave Safety Goggle |
| Brand | Sellstrom |
| Series | Odyssey II |
| Model | S80231 |
| Compliance Standard | ANSI/ISEA Z87.1+, OSHA 29 CFR 1910.133 |
| Lens Material | Gamma Ray-Resistant Polycarbonate |
| Lens Tint | Clear |
| Frame Material | Autoclave-Compatible Polymer (Non-Particle-Shedding) |
| Vent Type | Indirect Vent — No Direct Liquid Ingress Path |
| Sterilization Method | Autoclave (Steam) Compatible — 121°C / 15 PSI Standard Cycle |
| Radiation Resistance | Gamma Ray Resistant — Optical Stability Under Ionizing Exposure |
| Clean Room Rating | Yes — Non-Particle-Shedding Construction, ISO Class 5–8 |
| OTG Compatible | Yes — Fits Over Standard Prescription Eyewear |
| Protection Class | Chemical Splash, Impact, Particulate, Gamma Radiation |
| Primary Application | Pharmaceutical GMP, Nuclear Research, ISO Clean Rooms, BSL Facilities |
Laboratory Applications
Pharmaceutical sterile manufacturing facilities under FDA 21 CFR Part 211 GMP require goggle hardware sterilizable between uses without per-batch replacement. S80231 autoclave compatibility fulfills this requirement directly, enabling validated designated goggle programs within ISO Class 5 through 8 clean room environments. Radiation oncology research and nuclear medicine handling suites benefit from gamma-resistant optics that maintain optical qualification through sustained ionizing radiation exposure. A single SKU spanning clean room, autoclave, and radiation environments consolidates procurement documentation substantially.
Academic nuclear physics programs, radiopharmaceutical synthesis labs, and medical device sterile packaging operations all require PPE hardware that passes facility validation under sterilization and radiation exposure parameters. S80231 achieves dual validation across both gamma radiation and autoclave parameters within a single certified platform. BSL-2 and BSL-3 biocontainment environments requiring sterilizable goggle PPE for decontamination exit protocols represent an additional validated deployment context. Institutional volume orders are supported with B2B pricing and Net-30 terms through LabSupplies.com.
Lab Safety Eyewear Comparison: Why Choose LabSupplies.com?
| Feature | Sellstrom S80231 Odyssey II — LabSupplies.com | Standard Chemical Goggle |
|---|---|---|
| Compliance Standard | ANSI/ISEA Z87.1+ (High Impact) | ANSI Z87.1 Basic (tier varies) |
| Autoclave Sterilizable | Yes — Steam Cycle Validated at 121°C / 15 PSI | No — Warps/degrades under autoclave |
| Gamma Ray Resistance | Yes — Optically Stable Under Ionizing Radiation | No — Lens yellows under gamma exposure |
| Clean Room Compliant | Yes — Non-Particle-Shedding Construction | No — Not validated for ISO clean rooms |
| OTG Compatible | Yes — Confirmed | Rarely specified or validated |
| Price | $39.99 | $8–$20 (not fit-for-purpose in these environments) |
| B2B Support | Net-30, PO Accepted, Volume Pricing | Credit card only (most vendors) |
Academic and Institutional Pricing
LabSupplies.com provides tiered academic and institutional pricing on the Sellstrom S80231 Odyssey II Clean Room Goggle for qualified pharmaceutical manufacturers, nuclear research institutions, and government biosafety laboratory programs. Volume pricing activates at standard case quantities, with recurring contract terms available for ongoing sterile environment PPE programs. Net-30 payment terms are extended to all approved institutional purchasers. Submit your organization's credentials through the LabSupplies.com B2B portal for a formal volume quote and catalog assignment.
Product Documentation
- Technical compliance data, autoclave validation parameters, and product specification sheets available upon request through LabSupplies.com B2B account services.
- Sellstrom S80231 ANSI/ISEA Z87.1+ certification records verifiable through Sellstrom's official product compliance documentation portal.
Frequently Asked Questions
What autoclave sterilization parameters is the Sellstrom S80231 validated for?
The S80231 is designed to withstand standard gravity-cycle steam autoclave parameters at 121°C (250°F) and 15 PSI — the industry-standard cycle used across pharmaceutical GMP and biomedical research sterilization programs. Repeated cycling should not produce structural deformation, lens clouding, or peripheral seal failure. Post-autoclave inspection per your facility's equipment qualification SOP is required before returning goggles to active service. Cycle count limits should be tracked and documented within your facility's PPE validation records.
How does the S80231's gamma ray-resistant lens differ from standard polycarbonate goggles?
Standard polycarbonate lenses undergo measurable yellowing, haze increase, and optical transmission degradation when exposed to cumulative gamma radiation doses common in nuclear research and radiopharmaceutical environments. S80231's gamma ray-resistant optical construction uses stabilized polymer formulations that maintain ANSI Z87.1+ optical clarity requirements under sustained ionizing radiation exposure. Standard chemical goggles deployed in radiation environments will eventually fail optical clarity standards, creating a compliance gap that cannot be detected through visual inspection alone.
What ISO clean room classification does the Sellstrom S80231 support?
Sellstrom S80231 is constructed from non-particle-shedding materials appropriate for controlled contamination environments across ISO Class 5 through ISO Class 8 clean room classifications. Specific suitability confirmation against your facility's contamination control validation protocol is required, as clean room PPE qualification standards vary by regulatory framework. Pharmaceutical GMP environments should conduct formal suitability assessment under FDA 21 CFR Part 211 or EU Annex 1 guidance through your qualified person or facility validation team.