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ADVIA® Chemistry Reagent Wedge 20 mL

FDA UDI

Class I (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
ADVIA® Chemistry Reagent Wedge 20 mL FDA UDI
Generic Name
Assay container IVD, single-use FDA UDI
Device Name
ADVIA® Chemistry Reagent Wedge 20 mL FDA UDI
Model / Reference
10487137 FDA UDI
Description
ADVIA® Chemistry Reagent Wedge 20 mL FDA UDI

Identifiers

Catalog Number
073-0372-03 FDA UDI
Primary DI / UDI-DI
00630414601052 FDA UDI
510(k) Number
K990346 FDA UDI
FDA Product Code
JJE FDA UDI
GMDN Term
Assay container IVD, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2160 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Assay container IVD, single-use

ADVIA® Chemistry Reagent Wedge 20 mL by Siemens Healthcare Diagnostics — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Assay container IVD, single-use.

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 b062b9b9-2274-4489-b58d-bc58fb9a9768 36 fields · synced May 31, 2026