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SteriChek® Residual Peroxide Reagent Strips

FDA UDI

Class II (US FDA UDI)

by Hach Company

Identity

Trade Name
SteriChek® Residual Peroxide Reagent Strips FDA UDI
Generic Name
Medical device disinfection solution test strip FDA UDI
Device Name
Reagent test strips used to measure the concentration of residual peroxide in rinse water from dialyzers and dialysate lines disinfected with peroxide/peracetic acid. FDA UDI
Model / Reference
811905 FDA UDI
Description
Reagent test strips used to measure the concentration of residual peroxide in rinse water from dialyzers and dialysate lines disinfected with peroxide/peracetic acid. FDA UDI

Identifiers

Catalog Number
821971 FDA UDI
Primary DI / UDI-DI
00851575007075 FDA UDI
FDA Product Code
LIF FDA UDI
GMDN Term
Medical device disinfection solution test strip FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5820 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 3.25 Inch FDA UDI
Width — 0.2 Inch FDA UDI

SteriChek® Residual Peroxide Reagent Strips by Hach Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hach Company

Sources (1)

  • FDA UDI f71b3028-cca5-4ef7-ab9e-2acecbecf54b 38 fields · synced Jun 6, 2026