0.1 µm HEPA filtration
Only inline HEPA filter in this class with 0.1 µm pore size for IVF gas pathways.
Series: Embryo Shield
IVF Prime
Embryo Shield HEPA Inline Filter
0.1 µm HEPA inline gas filters — standard & Mild — MEA and pH tested
IVF ConsumablesConsumables
1 / 3Specifications
- Testing
- MEA and pH per lot · pressure test per unit
- Filtration
- HEPA inline · 0.1 µm pore size
- Variants
- Embryo Shield · Embryo Shield Mild
- Carbon media
- Washed coconut active carbon
- Replacement
- Every 6 months (recommended)
- Quality system
- ISO 13485:2016
Two variants: Embryo Shield (standard) and Embryo Shield Mild. Recommended replacement interval: 6 months.
Workflow: Gas Line Protection
Overview
Embryo Shield is the only HEPA inline filter with 0.1 µm pore size for IVF gas lines. Smaller pore size captures more particles in incubator supply gases. Each lot is MEA and pH tested; use has been associated with improved development to expanded blastocyst stage. Washed coconut active carbon (six sterile-water washes) offers higher absorption than coal-based carbon. A connector with check valve starts gas flow on connection and stops flow on disconnect. No adhesives or chemical binders in production. Each unit is pressure-tested. Plug-and-play connectors and ergonomic magnet holders simplify installation. Embryo Shield Mild provides the same technology in a mild configuration for sensitive workflows. Replace every 6 months for best results. Manufactured in an ISO 13485:2016 facility.
Applications
- Incubator and workstation gas line filtration
- Particle reduction in CO₂ and mixed gas supplies
- Scheduled IVF lab maintenance programs
Product features
MEA and pH tested lots
Each production lot is tested for embryo assay and pH compatibility.
Washed coconut active carbon
Carbon washed six times with sterile water for high absorption without coal-based media.
Gas flow safety
Check-valve connector allows immediate flow when connected and automatic stop when disconnected.
Adhesive-free construction
No adhesives or chemical materials in production — suited for medical gas use.
ISO 13485:2016 manufacturing
Pressure-tested units from a certified medical device quality system.
