← Back to catalogue

Water Hardness Test Strip

FDA UDI

Class I (US FDA UDI)

by Reprocessing Products Corp

Identity

Trade Name
Water Hardness Test Strip FDA UDI
Generic Name
Haemodialysis treatment kit FDA UDI
Device Name
Measures water hardness in the range of: 0.0, 5, 10, 17, 50, 120 ppm. Each bottle contains 50 test strips. FDA UDI
Model / Reference
K100-0102 FDA UDI
Description
Measures water hardness in the range of: 0.0, 5, 10, 17, 50, 120 ppm. Each bottle contains 50 test strips. FDA UDI

Identifiers

Catalog Number
K100-0102 FDA UDI
Primary DI / UDI-DI
00858293006342 FDA UDI
FDA Product Code
JRS FDA UDI
GMDN Term
Haemodialysis treatment kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2050 FDA UDI
Commercial Distribution
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

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Haemodialysis treatment kit

Water Hardness Test Strip by Reprocessing Products Corp — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Haemodialysis treatment kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Reprocessing Products Corp

Sources (1)

  • FDA UDI 68a7cc50-9b57-439e-8574-53224bf5ff43 34 fields · synced May 30, 2026