
Atellica IM Anti-Thyroglobulin | REF 10995461
Siemens Atellica IM Anti-Thyroglobulin (Anti-Tg) reagent pack, REF 10995461, for in vitro quantitative determination of anti-thyroglobulin autoantibodies on the Atellica IM analyzer.

The Siemens Atellica CH Direct Bilirubin reagent (REF 11097532) is an in vitro diagnostic assay designed for use on the Atellica CH Analyzer within the Atellica Solution platform. It enables quantitative determination of direct (conjugated) bilirubin in human serum and plasma to support assessment of hepatobiliary function.
Key Features
Ready-to-use liquid reagent formulation for the Atellica CH Analyzer
Optimized for integration within the Atellica Solution consolidated workflow
Designed for high-throughput clinical chemistry testing
Onboard stability and calibration intervals as defined in the official Instructions for Use
Barcoded reagent cartridge supporting automated handling and inventory tracking
Clinical Applications
Quantitative measurement of direct bilirubin in serum and plasma
Supports evaluation of liver function and hepatobiliary disorders
Aids differential assessment of jaundice (conjugated vs. unconjugated hyperbilirubinemia)
Routine clinical chemistry profiling in hospital and reference laboratories
Product Information
Brand: Siemens Healthineers
Product: Atellica CH Direct Bilirubin (DBIL)
REF/UPN: 11097532
Platform: Atellica CH Analyzer (Atellica Solution)
Sample Types: Serum and plasma
Format: Liquid reagent cartridge
Category: Siemens Atellica Reagents
Test count per pack / shelf life / storage conditions: Not specified in the located sources
Regulatory status: Refer to the official Siemens Healthineers Instructions for Use for your region
Tell us what product you need and share a few details.
We connect your request with the most relevant verified brands.
Relevant supplier options can respond with availability, documentation context, and quote details.
Practical answers for procurement teams reviewing this product page.
Include the exact product family, brand preference, REF/UPN code when available, required quantity, destination country, expected delivery timing and documentation expectations.
Yes. If alternatives are acceptable, mention equivalent brands, compatible models, size ranges and any non-negotiable requirements.
Related products are connected through structured catalog data such as brand, category, product family and country assignment.
No. This page supports sourcing and RFQ organization. Buyers must verify regulatory status, clinical suitability and procurement compliance independently.
Specific codes reduce ambiguity and help supplier teams identify product availability, packaging details and documentation faster.
Yes. The workflow is designed for hospitals, clinics, distributors, wholesalers, importers and procurement departments.
Yes. Products can be connected to multiple countries in the admin panel, and buyers can specify destination details in the RFQ form.
The request is stored with contact and procurement details so the sourcing conversation can be reviewed and followed up clearly.