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RAPIDLab® Deproteinizer

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
RAPIDLab® Deproteinizer FDA UDI
Generic Name
Wash/cleaning solution IVD, automated/semi-automated system FDA UDI
Device Name
RAPIDLab® Deproteinizer for in vitro diagnostics use with the RAPIDLab® series analyzers (Pack 10) FDA UDI
Model / Reference
10309775 FDA UDI
Description
RAPIDLab® Deproteinizer for in vitro diagnostics use with the RAPIDLab® series analyzers (Pack 10) FDA UDI

Identifiers

Catalog Number
105610 FDA UDI
Primary DI / UDI-DI
00630414055909 FDA UDI
510(k) Number
K962021 FDA UDI
FDA Product Code
CGZ FDA UDI
JGS FDA UDI
CHL FDA UDI
JFP FDA UDI
CEM FDA UDI
GMDN Term
Wash/cleaning solution IVD, automated/semi-automated system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1170 FDA UDI
862.1665 FDA UDI
862.1120 FDA UDI
862.1145 FDA UDI
862.1600 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Wash/cleaning solution IVD, automated/semi-automated system

RAPIDLab® Deproteinizer by Siemens Healthcare Diagnostics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wash/cleaning solution IVD, automated/semi-automated system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 02113768-a709-43c4-990d-c8b72c045706 37 fields · synced May 30, 2026