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Washing Solution Concentrate

FDA UDI

Class II (US FDA UDI)

by Bio-Rad Medical Diagnostics GmbH

Identity

Trade Name
Washing Solution Concentrate FDA UDI
Generic Name
Buffered wash solution IVD FDA UDI
Device Name
Washing solution for Solidscreen II assays for use with TANGO instruments FDA UDI
Model / Reference
848000091 FDA UDI
Description
Washing solution for Solidscreen II assays for use with TANGO instruments FDA UDI

Identifiers

Catalog Number
848000091 FDA UDI
Primary DI / UDI-DI
07611969965304 FDA UDI
FDA Product Code
KSZ FDA UDI
GMDN Term
Buffered wash solution IVD FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.9175 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

Yes

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

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: Buffered wash solution IVD

Washing Solution Concentrate by Bio-Rad Medical Diagnostics GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Buffered wash solution IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3f1035c6-96e3-4ab5-b6f4-afb184b3a498 36 fields · synced May 30, 2026