| MOQ: | 1 set |
| Price: | Negotiable |
| Standard Packaging: | Plywood packing |
| Delivery Period: | 5~8 working days |
| Payment Method: | L/C,T/T |
| Supply Capacity: | 500 sets/month |
Product Introduction
TOC-10 adopts ultraviolet oxidation and direct conductivity difference detection technology, featuring high detection accuracy and short response time. The testing methods are satisfied with the requirements of FDA, Chinese Pharmacopoeia and GMP regulations, as well as the requirements of USP and EP,It can meet the offline detection requirements for deionized water such as pharmaceutical water (injection water and purified water), ultra-pure water, etc.
Application Area
Pharmaceutical industry
Medical device industry
Food and beverage industry
Environmental protection industry
Product Features
1. No nitrogen, oxygen, acid reagents, or oxidants required; simple operation and low cost.
2. Suitable for offline laboratory use, meeting the testing and cleaning validation requirements for OCC in water for injection and purified water.
3. Instrument software provides audit trails, simplifying validation and facilitating retrieval.
4. High level of intelligence, equipped with an autosampler; system adaptability validation can be completed automatically.
5. Limit alarm design; the instrument automatically alarms when the test sample exceeds the specified limit.
6. Complies with the testing protocols stipulated in the new edition of the National Pharmacopoeia and can provide IQ/OQ/PQ validation services.
7. Equipped with electronic signature, audit trail, and original data traceability functions, meeting the validation requirements of GMP, the Chinese Pharmacopoeia, and 21CFRPART11 computerized systems.
Technical parameters
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TOC-10 total organic carbon analyzer |
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Measurement Range |
0.001mg/L~1.5 mg/L(1~1500ppb) |
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Electrical Conductivity Detection Range |
0.055μs/cm~8μs/cm |
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Measurement Accuracy |
±3% |
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Resolution |
0.001mg/L |
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RSD |
Repeatability≤3% |
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Analysis Time |
Continuous Analysis |
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Response Time |
Within 5 minutes |
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Detection Limit |
0.001 mg/L |
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Sample Temperature |
1-99℃ |
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Application Scope |
Offline laboratory, cleaning verification |
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Operating System |
Windows System |
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Audit Trail |
Multiple event records |
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Permission management |
Username and password login, 4-level permissions, meeting FDA 21CFR PART 11 requirements |
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Printing function |
Built-in micro printer |
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History record |
Unlimited storage capacity |
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Data backup |
Support for USB drive export of data |
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Display screen |
12-inch color touch screen |
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Communication module |
Customizable (4-20)mA, RS485, 12V alarm output Sample addition: Standard configuration |
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Scheme setting |
Standard configuration |
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Data backup |
Manual or automatic backup |
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Screen lock function |
Standard feature |
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Information alarm |
Standard feature |
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Power Supply Requirements/Power Consumption |
100 - 240 VAC, 50Hz, 120W |
Adequate Supply
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