CiDehol ST Sterile 70% IPA Solution with WFI
• Sterile, ready-to-use 70% isopropyl alcohol (IPA) solution made with Water for Injection (WFI)
• Ideal for cleanroom use
• Solution is filtered to 0.2 µm to remove particulate contamination
• It evaporates completely, with no rinsing required
• Made according to USP specifications and packaged in an ISO Class 5 (FED-STD-209E Class 100/M3.5) cleanroom
• Each lot undergoes a bacterial endotoxin test to ensure that the product meets or exceeds Water-for-Injection quality in endotoxin limits, and each lot also undergoes a USP 14-day sterility test
• Each case is shipped with lot specific documentation which details QC, irradiation, sterility, and bacterial endotoxin limits
• Each lot is double-bagged and gamma-irradiated to ensure sterility
Image(s) are representative of the product group and not necessarily the individual product.
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• Ideal for cleanroom use
• Solution is filtered to 0.2 µm to remove particulate contamination
• It evaporates completely, with no rinsing required
• Made according to USP specifications and packaged in an ISO Class 5 (FED-STD-209E Class 100/M3.5) cleanroom
• Each lot undergoes a bacterial endotoxin test to ensure that the product meets or exceeds Water-for-Injection quality in endotoxin limits, and each lot also undergoes a USP 14-day sterility test
• Each case is shipped with lot specific documentation which details QC, irradiation, sterility, and bacterial endotoxin limits
• Each lot is double-bagged and gamma-irradiated to ensure sterility
Image(s) are representative of the product group and not necessarily the individual product.
• Sterile, ready-to-use 70% isopropyl alcohol (IPA) solution made with Water for Injection (WFI)
• Ideal for cleanroom use
• Solution is filtered to 0.2 µm to remove particulate contamination
• It evaporates completely, with no rinsing required
• Made according to USP specifications and packaged in an ISO Class 5 (FED-STD-209E Class 100/M3.5) cleanroom
• Each lot undergoes a bacterial endotoxin test to ensure that the product meets or exceeds Water-for-Injection quality in endotoxin limits, and each lot also undergoes a USP 14-day sterility test
• Each case is shipped with lot specific documentation which details QC, irradiation, sterility, and bacterial endotoxin limits
• Each lot is double-bagged and gamma-irradiated to ensure sterility
Image(s) are representative of the product group and not necessarily the individual product.
• Ideal for cleanroom use
• Solution is filtered to 0.2 µm to remove particulate contamination
• It evaporates completely, with no rinsing required
• Made according to USP specifications and packaged in an ISO Class 5 (FED-STD-209E Class 100/M3.5) cleanroom
• Each lot undergoes a bacterial endotoxin test to ensure that the product meets or exceeds Water-for-Injection quality in endotoxin limits, and each lot also undergoes a USP 14-day sterility test
• Each case is shipped with lot specific documentation which details QC, irradiation, sterility, and bacterial endotoxin limits
• Each lot is double-bagged and gamma-irradiated to ensure sterility
Image(s) are representative of the product group and not necessarily the individual product.
Shipping Information
DOT: UN1219, Isopropanol, solution, 3, PG II
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| QAF481 | Authorized Purchaser form |
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