← Back to catalogue

ADVIA® Chemistry Direct Bilirubin_2 DBIL_2 Reagents

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
ADVIA® Chemistry Direct Bilirubin_2 DBIL_2 Reagents FDA UDI
Generic Name
Conjugated (direct) bilirubin IVD, kit, spectrophotometry FDA UDI
Device Name
Bilirubin Direct - ADVIA Chem. - RGT - 4x672 tests FDA UDI
Model / Reference
10341114 FDA UDI
Description
Bilirubin Direct - ADVIA Chem. - RGT - 4x672 tests FDA UDI

Identifiers

Catalog Number
2188390 FDA UDI
Primary DI / UDI-DI
00630414513065 FDA UDI
510(k) Number
K053132 FDA UDI
FDA Product Code
JFM FDA UDI
GMDN Term
Conjugated (direct) bilirubin IVD, kit, spectrophotometry FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1110 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: Conjugated (direct) bilirubin IVD, kit, spectrophotometry

ADVIA® Chemistry Direct Bilirubin_2 DBIL_2 Reagents by Siemens Healthcare Diagnostics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Conjugated (direct) bilirubin IVD, kit, spectrophotometry.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI faecae4d-6bed-4b78-9212-ad69b02a0803 37 fields · synced May 30, 2026