Identity
- Trade Name
- Atellica CH Diazo Direct Bilirubin (D_DBil) FDA UDI
- Generic Name
- Conjugated (direct) bilirubin IVD, kit, spectrophotometry FDA UDI
- Device Name
- Atellica CH Diazo Direct Bilirubin (D_TBil) FDA UDI
- Model / Reference
- 11537219 FDA UDI
- Description
- Atellica CH Diazo Direct Bilirubin (D_TBil) FDA UDI
Identifiers
- Catalog Number
- 11537219 FDA UDI
- Primary DI / UDI-DI
- 00630414614755 FDA UDI
- 510(k) Number
- K223078 FDA UDI
- FDA Product Code
- CIG 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
Atellica CH Diazo Direct Bilirubin (D_DBil) 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.
- Bilirubin Direct Gen.2 (Doumas standardization) — Roche Diagnostics Corp. · Class II
- Direct Bilirubin LiquiColor® — STANBIO LABORATORY, L.P. · Class II
- ENVOY 500 DIRECT BILIRUBIN REAGENT KIT — VITALSCIENTIFIC
- DIRECT BILIRUBIN-SL Assay — Sekisui Diagnostics, LLC · Class II
- DBIL Reagent Kit — Medica Corp. · Class II
- Advanced Instruments BR2 Hydrochloric Acid — Advanced Instruments, LLC · Class II
- Advanced Instruments BR2 Sulfanilic Acid — Advanced Instruments, LLC · Class II
- Thermo Scientific — Fisher Diagnostics · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Siemens Healthcare Diagnostics
Sources (1)
- FDA UDI fe2e3cd7-031b-45dd-b084-8487e10acf57 37 fields · synced May 30, 2026