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Sterichek® Total Chlorine Test Kit Refill

FDA UDI

Class II (US FDA UDI)

by Hach Company

Identity

Trade Name
Sterichek® Total Chlorine Test Kit Refill FDA UDI
Generic Name
Haemodialysis dialysate water chlorine test kit FDA UDI
Device Name
DPD reagent powder pillows refill, used with reagent test kit to measure low levels of total chlorine in feed water used to prepare dialysate. FDA UDI
Model / Reference
811902 FDA UDI
Description
DPD reagent powder pillows refill, used with reagent test kit to measure low levels of total chlorine in feed water used to prepare dialysate. FDA UDI

Identifiers

Catalog Number
811903 FDA UDI
Primary DI / UDI-DI
00851575007068 FDA UDI
FDA Product Code
FIP FDA UDI
MSY FDA UDI
GMDN Term
Haemodialysis dialysate water chlorine test kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5665 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

Yes

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
Weight — 0.150 Gram FDA UDI

Sterichek® Total Chlorine Test Kit Refill 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 e9e477f0-3d73-43d5-add6-3728d3a21c5b 38 fields · synced Jun 1, 2026