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N Supplementary Reagent/Precipitation

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics Products Ltd

Identity

Trade Name
N Supplementary Reagent/Precipitation FDA UDI
Generic Name
Buffered isotonic saline reagent IVD FDA UDI
Device Name
Supplementary reagent for multiple protein assays on Siemens systems FDA UDI
Model / Reference
10446458 FDA UDI
Description
Supplementary reagent for multiple protein assays on Siemens systems FDA UDI

Identifiers

Catalog Number
OUMU15 FDA UDI
Primary DI / UDI-DI
00842768011443 FDA UDI
510(k) Number
K860894 FDA UDI
FDA Product Code
CFN FDA UDI
GMDN Term
Buffered isotonic saline reagent IVD FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5510 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: Buffered isotonic saline reagent IVD

N Supplementary Reagent/Precipitation by Siemens Healthcare Diagnostics Products Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Buffered isotonic saline reagent IVD.

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 60ee582d-d920-4e2b-a9e1-5651d0b5b9c6 37 fields · synced Jun 8, 2026