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Thermo Scientific™ Nalgene™ Square PETG Platinum Certified Clean Media Bottle
Thermo Scientific™ Nalgene™ Square PETG Platinum Certified Clean Media Bottles are certified and lot-to-lot tested to contain less than 1/3 the particulates allowable according to USP <788> to limit potential particulate contamination.
108234.84 DKK - 151825.51 DKK
Specifications
For Use With (Application) | Media/Buffer Preparation ​, Media/Buffer Storage, Sampling, Storage, Transportation ​, Validation Testing, Drug Substance, Drug Product |
---|---|
Sterility | Sterile |
Temperature Range (Metric) | -70°C to 70°C |
Low Particulate | <1/3 USP <788> (Ultralow particulate) |
Certifications/Compliance | ISO 13485:2003, 21 CFR 177.1520, USP Class VI |
Product Code | Brand | Capacity (Metric) | Price | Quantity & Availability | ||||||
---|---|---|---|---|---|---|---|---|---|---|
Product Code | Brand | Capacity (Metric) | Price | Quantity & Availability | ||||||
16450611
|
Thermo Scientific™
CE-N2035-0005 |
5 mL |
108234.84 DKK
Pack of 416 |
Estimated Shipment: 26-01-2026
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16460611
|
Thermo Scientific™
CE-N2035-0020 |
20 mL |
151825.51 DKK
Pack of 504 |
Estimated Shipment: 21-01-2026
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Description
Products are washed with USP Water for Injection and handled post-washing in Class 5 clean rooms with Class 4 packaging/inspection hoods to produce these very low particulate products. Certified and lot-to-lot tested to contain less than 1/3 the particulates allowable according to USP <788> to limit potential particulate contamination. Sterile, ready-to-use products with a Sterility Assurance Level of 10-6 inside the container/closure, including two heat-sealed sterile barriers to protect product prior to use.
- Sterile to 10-6 SAL
- Non-pyrogenic and non-cytotoxic
- Leakproof High Density Polyethylene (HDPE) closures
- Serum Vials are packed in shrink-wrapped trays with closures attached
- Manufactured in compliance with ISO 13485:2003 quality requirements
Specifications
Media/Buffer Preparation ​, Media/Buffer Storage, Sampling, Storage, Transportation ​, Validation Testing, Drug Substance, Drug Product | |
-70°C to 70°C | |
ISO 13485:2003, 21 CFR 177.1520, USP Class VI |
Sterile | |
<1/3 USP <788> (Ultralow particulate) | |
Media Bottle |
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