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Dade® Sickle-Sol Test

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics Products Ltd

Identity

Trade Name
Dade® Sickle-Sol Test FDA UDI
Generic Name
Haemoglobin S (HbS) IVD, reagent FDA UDI
Device Name
Qualitative Solubility for sickling hemoglobin FDA UDI
Model / Reference
10459402 FDA UDI
Description
Qualitative Solubility for sickling hemoglobin FDA UDI

Identifiers

Catalog Number
B4585-5 FDA UDI
Primary DI / UDI-DI
00630414976365 FDA UDI
FDA Product Code
GHM FDA UDI
GMDN Term
Haemoglobin S (HbS) IVD, reagent FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.7825 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

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: Haemoglobin S (HbS) IVD, reagent

Dade® Sickle-Sol Test by Siemens Healthcare Diagnostics Products Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Haemoglobin S (HbS) IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f58becef-3e53-4443-9e07-cf8628454fc5 36 fields · synced May 30, 2026